US008551526B2

(12) United States Patent (10) Patent No.: US 8,551,526 B2

Johnston et al. (45) Date of Patent: *Oct. 8, 2013

(54) PREPARATION OF DRUG PARTICLES USING 6,077,543 A 6/2000 Gordon et al. ................ 424/489
EVAPORATION PRECIPITATION INTO 33 . ck 39 SE et al . . . . . . . . . . . . . . . 424/451
-w OSO ca.
AQUEOUS SOLUTIONS 6,908,626 B2 * 6/2005 Cooper et al. ................ 424/489
(75) Inventors: Keith P. Johnston, Austin, TX (US); FOREIGN PATENT DOCUMENTS
Robert O. Williams, III, Austin, TX
(US); Xiaoxia Chen, Austin, TX (US) WO 9714407 4f1997
WO 98.29096 7, 1998
(73) Assignee: Board of Regents, The University of WO O247659 A2 6, 2002
Texas System, Austin, TX (US) OTHER PUBLICATIONS
(*) Notice: Subject to any disclaimer the term of this Liversidge et al., “Particle size Reduction for Improvement of Oral
patent is extended or adjusted under 35 Bioavailability of Hydrophobic Drugs: I. Absolute Oral Bioavail
U.S.C. 154(b) by 0 days. ability of Nanocrystalline Danazol in Beagle Dogs”. International
This patent is Subject to a terminal dis- Journal of Pharmaceutics 125 (1995) 91-97.*
claimer. True et al. A novel particle engineering technology to enhance dis
Solution of poorly water Soluble drugs: spray-freezing into liquid,
(21) Appl. No.: 10/266,998 European Journal of Pharmaceutics and Biopharmaceutics 54 (2002)
271-28O.*
(22) Filed: Oct. 8, 2002 Sherif et al., Characterization and bioavailability of danazol
hydroxypropyl B-cyclodextrin copreciptates, International Journal
(65) Prior Publication Data of Pharmaceutics 128 (1996) 45-54.*
Reverchon, E. et al., “Supercritical Antisolvent Precipitation of
US 2004/OO67251A1 Apr. 8, 2004 Micro- and Nano-Particles,” Journal of Supercritical Fluids, vol. 15.
O O 1999, pp. 1-21.
Related U.S. Application Data Young, T. J. et al., “Rapid Expansion from Supercritical to Aqueous
(63) Continuation-in-part of application No. 09/808.332. Solution to Produce Submicron Suspensions of Water-Insoluble
filed on Mar. 14, 2001, now Pat. No. 6,756,062. Drugs. Biotechnol Prog, vol. 16, 2000, pp. 402-407.
PCT Publication of International Search Report for PCT/US2001/
(60) Provisional application No. 60/245,479, filed on Nov. 051337 Dated Jun. 20, 2002, 3 pp.
3, 2000.
* cited by examiner
(51) Int. Cl.
A6 IK 9/16 (2006.01) Primary Examiner — Michael G. Hartley
A 6LX 9/50 (2006.01) Assistant Examiner — Nabila Ebrahim
A6 IK 9/26 (2006.01) (74) Attorney, Agent, or Firm — Chainey P. Singleton;
A6 IK 8/00 (2006.01) Edwin S. Flores; Chalker Flores, LLP
(52) U.S. Cl.
USPC ........... 424/489: 424/494; 424/496; 424/497; (57) ABSTRACT
424/7O.19 A method for preparing poorly water Soluble drug particles is
(58) Field of Classification Search disclosed. The method comprises dissolving a drug in at least
USPC .. .. . .. . .. .. . . . . . . . ... 424/489 one organic solvent to form a drug/organic mixture, spraying
See application file for complete search history. the drug/organic mixture into an aqueous Solution and con
currently evaporating the organic solvent in the presence of
(56) References Cited the aqueous solution to form an aqueous dispersion of the
U.S. PATENT DOCUMENTS drug particles. The resulting drug particles are in the nanom
eter to micrometer size range and show enhanced dissolution
5,145,684. A * 9/1992 Liversidge et al. ........... 424/489 rates and reduced crystallinity when compared to the unproc
5,686,133 A * 1 1/1997 Amidon et al. .............. 427,222 essed drug. The present invention additionally contemplates
5,766,635 A 6/1998 Spenleuhauer et al. products and processes for new drug formulations of
5,773,025 A * 6/1998 Baichwal ...................... 424/458 insoluble drug particles having high dissolution rates and
5,795,594 A 8, 1998 York et al. ... ... 424/489
5,851,453 A 12, 1998 Hanna et al. ...................... 264.5 extremely high drug-to-excipient ratios.
5,985,248 A 11/1999 Gordon et al. ... ... 424/46
6,001,336 A * 12/1999 Gordon ........ ... 424/46 5 Claims, 11 Drawing Sheets
U.S. Patent Oct. 8, 2013 Sheet 1 of 11 US 8,551,526 B2

F.G. 1

FIG. 2
U.S. Patent Oct. 8, 2013 Sheet 2 of 11 US 8,551,526 B2

FIG. 3

0 50 100 150 200

Time (min)
-(- BulkTAA -A - Example 28
-- Example 27 -o- Example 29

100

80

60

40

20

O
O 15 30 45 60
Time (min)
-o-Bulk Carbamazepine - A - Example 31
-- Example 30 -O-Example 32
U.S. Patent Oct. 8, 2013 Sheet 3 of 11 US 8,551,526 B2

FIG 5
U.S. Patent Oct. 8, 2013 Sheet 4 of 11 US 8,551,526 B2

F.G. 6

100
90
80
70
60
50
40
30
20
10
O 20 40 60
Time (min)
-- Example 34 - A - Example 36
-o- Example 35 -o- Example 37
U.S. Patent Oct. 8, 2013 Sheet 5 of 11 US 8,551,526 B2

FG. 7

the apparatus of EPAS

pure solvent
reservoir

drug solution
reservoir

T-thermocouple;
P-pressure regulator;
H-BPLC pump
U.S. Patent Oct. 8, 2013 Sheet 6 of 11 US 8,551,526 B2

F.G. 8

the x-ray profile of danazol systems

8000

6000 PWP4OSDS

-6 PVP4OT-Pluronic F27
so P1
-
PVP 4OTOCA
Proro F27
OCA
2000 ? PVP K-15
PVP 4OT
BUK carazo

3. O 17 24 3. 38 45
U.S. Patent Oct. 8, 2013 Sheet 7 of 11 US 8,551,526 B2

FIG. 9 (a)
danazol systems with high dissolution rate
OO

80

S 60
-E-Da-PVP40
40 -e-Dan-PWPK-5
al-Da-PVP4OTSOS
-O-Bulk Darazo
2O

O
O 2O 40 60 BO OO 120
Time (min)

danazol systems with low dissolution rate FIG 9(b)

20

OO

80
s-O-Bulk danazol
S -e-Puronic F27
-E-DCA
-0-PVP4OT-Pluronic F27
a--PVP 400CA
20
U.S. Patent Oct. 8, 2013 Sheet 8 of 11 US 8,551,526 B2

F.G. 10
Particle redispersibility in the stability study period
30

25 -O-PVPK-15+Danazol (no US)

g
E. -O-PVPK-15+Danazo (15s US)
20
--PVP4OTDanazol (no US)
5 --PVP4OT+Danazoi (15s US)
e

-0-PVP4OTSDS-Danazo (no US)

O
-0-PVP 40TSDS-Danazo (15s US)
5
O 2
time (week)
F.G. 11

The x-ray peak height of danazol samples during stability study

3000

2000

a-O-PWPK-5danazol
She OOO --PVP 40-danazol
-A-PVP4OTSOS+darazo
O
O 1 2
Tirne (week)
U.S. Patent Oct. 8, 2013 Sheet 9 of 11 US 8,551,526 B2

F.G. 12

Surface area of danazol systems during stability study

O

g 8
5 s
3 4
. s-d-PWPK-5-danazol
s
Clo 2 e-PVP4OT.canazo
s-O-PVP4OTSDS-danazol
O
O 2
Time (week)

FIG. 13 (a)
Dissolution profile of system danazol--PVP4OT+SDS during stability study
OO

--Dan-PVP40+SDS (O wks)
-0-Dan-PVP40+SDS (1 wiks)
-o-Dan-PVP40+SDS (2 wiks)

O 30 60 90 20

Time (min)
U.S. Patent Oct. 8, 2013 Sheet 10 of 11 US 8.551,526 B2

FIG. 13(b)
Dissolution profile of system danazol--PVPK-15 during

ge 60 --Dan-PVP15 (Owks)
40 -0-Dan-PVP15 (1 wks)
-O-Dan-PVP15(2wks)
20

O
O 30 60 90 2O
Time (m
FIG. 13 (c) me (min)
Dissolution profile of system danazol--PVP 40T during stability study
OO

80

60 --Dan+PVP400 wks)
-0-Dan-PVP40 (1 wiks)
-O-Dan+PVP40 (2wks)

O 30 60 90 f2O
U.S. Patent Oct. 8, 2013 Sheet 11 of 11 US 8,551,526 B2

F.G. 14

Figure 8: SEM pictures of danazol samples

PVP K-15 Danazol PWP4OT +Danazol

PWP 40T-I-SOS Darazo

 US 8,551,526 B2
1. 2
PREPARATION OF DRUG PARTICLES USING more difficult to control the particle morphology. Further
EVAPORATION PRECIPITATION INTO more, in all of these teachings, the useful excipients are Sug
AQUEOUS SOLUTIONS ars, salts, pectin and citric acid, which are not good stabilizers
for preventing growth of particles during the spray process.
This application is a continuation-in-part of U.S. applica U.S. Pat. Nos. 5,795,594 and 5,851,453 teach the use of
tion Ser. No. 09/808,332 filed Mar. 1, 2001 (U.S. Pat. No. compressed fluid antisolvents to form drug particles in the
6.356,062 granted on Jun. 29, 2004) which claims priority to micron-size range. This process has been called Precipitation
U.S. application Ser. No. 60/245,479 filed on Nov. 3, 2000, using Compressed Antisolvents (PCA), Solution-Enhanced
under Title 35 of the United States Code section 120. Dispersion of Solids (SEDS) and Supercritical AntiSolvent
10
FIELD OF THE INVENTION
process (SAS). In most cases this process does not utilize
water due to the low solubility of water in compressed carbon
The present invention relates to drug particles and methods dioxide, so that it is difficult to use water-soluble excipients
for their preparation. More particularly, the present invention with this process. However, in Some cases, this process is able
relates to the preparation of drug particles utilizing evapora 15 to use water by flowing an organic drug Solution, an aqueous
tive precipitation into aqueous solutions. Solution and a second organic Solvent such as ethanol into
compressed carbon dioxide. The ethanol is needed to extract
DESCRIPTION OF RELATED ART the water into the CO2 phase. In this process it is difficult to
control the particle size due to the complexity of the mixing of
Bioavailability is a term meaning the degree to which a the three streams in the jet. Also, the particles must be recov
drug becomes available to the target tissue after being admin ered from a high pressure vessel, and high ratios of CO2 to
istered to the body. Poor bioavailability is a significant prob drug are necessary. Moreover, as the water contacts CO2, the
lem encountered in the development of pharmaceutical com pH in the water reaches 3, which can be detrimental to drug
positions, particularly those containing an active ingredient stability and interactions with excipients.
that is poorly soluble in water. Poorly water soluble drugs 25 Young et al., Rapid Expansion from Supercritical to Aque
tend to be eliminated from the gastrointestinal tract before ous Solution to Produce Submicron Suspensions of Water
being absorbed into the circulation. Insoluble Drugs, Biotechnol. Prog. 2000, 16, 402-407, teach
It is known that the rate of dissolution of a particulate drug the formation of poorly water soluble drug particles by rapid
can increase with increasing Surface area, that is, decreasing expansion of Supercritical fluid Solutions into water, the
particle size. Efforts have been made to control the size and 30
supercritical fluid was carbon dioxide above its critical tem
size range of drug particles in pharmaceutical compositions perature. The solubility of drugs in carbon dioxide and other
For example, wet milling techniques have been used, as Supercritical fluids such as ethane and propane is typically
described in U.S. Pat. No. 5,145,684. However, such wet
milling techniques exhibit problems associated with contami very small. It is difficult to add water soluble stabilizers and
nation from the grinding media. It is difficult to produce 35 excipients in spray antisolvent processes (PCA, SAS or
highly uniform Submicron particles with wet milling and SEDS) into carbon dioxide due to the low solubility of water
Solids milling, and handling can be time consuming. Large in CO2. Reverchon E. Supercritical Antisolvent Precipita
amounts of Surfactants are needed for stabilization resulting tion of Micro-and Nano-particles, J. Supercrit. Fluid., 1999,
in Small drug-to-excipient ratios. Moreover, exposing a drug 15, 1-21. These antisolvent processes require large ratios of
Substance to mechanical shear or high temperatures for pro 40 carbon dioxide to drug and the use of a high pressure vessel
longed periods can cause the drug to lose its activity. for recovery of product. Even when an aqueous and two
Spray drying into vapor is another method used to form organic solutions are sprayed through a coaxial nozzle, the
micron sized drug particles. Spray drying is used commonly process is Subject to many of the limitations discussed above
to formulate dry pharmaceutical powder. In most cases, either for spray drying organic and aqueous phases through coaxial
hydrophilic drugs in aqueous Solution or poorly water soluble 45 nozzles. As the water dissolves into the ethanol-carbon diox
drugs in organic Solution are sprayed, which approaches do ide mixture, it is no longer available to solvate stabilizers to
not offer a means to simultaneously spray a poorly water prevent particle growth. Therefore this process is limited to
soluble drug and water soluble excipient. relatively few drugs.
U.S. Pat. No. 5,985,248 teaches dissolving a hydrophilic It would be an advantage in the art of preparation of drug
excipient, or stabilizer, and a hydrophobic drug in a cosolvent 50 particles to provide a method which allows for easy control of
system such as water:ethanol, and spray drying the system particle size and morphology and which is applicable to a
into vapor. U.S. Pat. No. 6,001.336 teaches suspending a wide breadth of drug substances.
hydrophobic drug in an aqueous solution containing a hydro An additional challenge for poorly water soluble drugs is to
philic stabilizer, and spray drying the Suspension into vapor. achieve high dissolution rates with a high drug-to-excipient
U.S. Pat. No. 6,077.543 and WO 98/29096 teach atomizing 55 ratio or high payload. From a therapeutic point of view, drug
an organic and an aqueous solution together into a vapor. In formulations with high drug-to-excipient ratios, or payloads,
all of these teachings, drug particles in the micron size range have many advantages. First, such formulations allow an
are formed. It is difficult to produce sub-micron particles by effective dose to be used to produce high levels of local drug
these technique due to growth of the drug particles during the concentration with greater therapeutic efficiency. Second,
Solvent evaporation. As the water evaporates it will no longer 60 high drug loading results in less coadministration of the
solvate hydrophilic stabilizers. Solvation of the stabilizer is excipients, thereby minimizing potential biological reaction
needed for it to be able to prevent growth of the drug particles. to such excipients. Excipients are used to increase the disso
As a result, growth of the drug particles is not likely to be lution rates of poorly water soluble drugs. Known techniques
inhibited by the stabilizer and the particle size is typically use a drug to excipient ratio on the order of 1:1, for example,
greater than 1 micron. Moreover, in all of these teachings, the 65 the Nanocrystal technology of Elan pharmaceuticals.
precipitation of Surfactant, or other excipient, and stabilizers Therefore, there remains a need for drug formulations and
occur simultaneously in the coaxial nozzle, and it is much techniques that allow for enhanced drug potency leading to
 US 8,551,526 B2
3 4
greater therapeutic efficiency for poorly water Soluble drugs. FIG. 6 is a graph showing improved dissolution rates for
Accordingly, achieving immediate release with a high drug particles of the present invention.
to-excipient ratio is desirable. FIG. 7 is a depiction of an EPAS apparatus, where T-ther
mocouple, P-pressure regulator, and H=HPLC pump.
SUMMARY OF THE INVENTION FIG. 8 is an X-ray profile of danazol systems.
FIG. 9(b) is a graph showing danazol systems with low
In one aspect, the present invention is a method for prepar dissolution rates.
ing poorly water soluble drug particles comprising the steps FIG. 10 is a graph reflecting the particle redispersibility in
of dissolving a drug in at least one organic solvent to form a the stability study period.
drug/organic mixture; spraying the drug/organic mixture into 10 FIG. 11 is a graph showing the X-ray peak height of danazol
an aqueous Solution; and concurrently evaporating the samples during the Stability study.
organic solvent in the presence of the aqueous solution to FIG. 12 is a graph depicting the Surface area of danazol
form an aqueous dispersion of the drug particles. systems during the stability study.
In a second aspect, the present invention is poorly water FIG. 13(a) is a graphic illustration of the dissolution profile
soluble drug particles having an average particle diameter of
15 of system danazol--PVP 40T+SDS during stability study.
from 50 nanometers to 20 microns, the drug particles being FIG. 13(b) is a graphic illustration of the dissolution profile
prepared by a process comprising the steps of dissolving the of system danazol--PVP K-15 during stability study.
drug in at least one organic solvent to form a drug/organic FIG. 13(c) is a graphic illustration of the dissolution profile
of system danazol--PVP 40T during stability study.
mixture; spraying the drug/organic mixture into an aqueous FIG. 14 are SEMs showing danazol samples.
Solution; and concurrently or rapidly evaporating the organic
Solvent in the presence of the aqueous solution to form an DETAILED DESCRIPTION OF THE INVENTION
aqueous dispersion of the drug particles.
In another aspect, the present invention provides for drying FIG. 1 is a schematic diagram illustrating one embodiment
or otherwise removing water or other excipients from the 25 ofan apparatus useful for the process of the present invention.
aqueous dispersion of drug particles. The drying may be As shown, tank 11 contains a drug/organic mixture.
accomplished by any known method of removing water or The drug/organic mixture is formed by dissolving a drug in
other excipient(s) from particles including, but not limited to, at least one organic solvent. The resulting drug/organic mix
lyophilization, vacuum drying, spray drying, or the like. In ture can be a solution, an emulsion or a microemulsion.
another aspect of the invention, water removed is facilitated 30 The drug which can be used in the process of the present
prior to drying, Such as for example and without limitation, by invention can be any poorly water Soluble drug. Suitable drug
centrifugation, filtration, settling, anti-solvent or flocculating substances can be selected from a variety of known classes of
agent, a gelation agent, an adsorbent, a solid matrix or Solid drugs including, for example, analgesics, anti-inflammatory
particles that the particles adhere to, or the like. agents, anthelmintics, antianginal agents, anti-arrhythmic
Another aspect of the present invention provides poorly 35 agents, antibiotics (including penicillins), anticoagulants,
water Soluble drug particles with high drug:excipient ratios: antidepressants, antidiabetic agents, antiepileptics, antigona
high dissolution rates; high potency; or high Surface areas. In dotropins, antihistamines, antihypertensive agents, antimus
an exemplary case herein, formulation of Such micron or carinic agents, antimycobacterial agents, antineoplastic
Sub-micron size drug particles were produced by evaporative agents, immunosuppressants, antithyroid agents, antiviral
precipitation into an aqueous Solution containing the excipi 40 agents, anxiolytic sedatives (hypnotics and neuroleptics),
ent. astringents, beta-adrenoceptor blocking agents, blood prod
In certain aspects, the present invention utilizes evapora ucts and Substitutes, cardiacinotropic agents, contrast media,
tive precipitation into aqueous solutions (EPAS) to form cortieosterioids, cough Suppressants (expectorants and
micron to Sub-micron sized drug particles, leading to mucolytics), diagnostic agents, diagnostic imaging agents,
increased bioavailability relative to larger particles. The pro 45 diuretics, dopaminergics (antiparkinsonian agents), haemo
cess of the present invention has applicability to a wide range statics, immunosuppressive cyclic oligopeptides, immuno
of drug Substances as several Solvents may be chosen to logical agents, lipid regulating agents, muscle relaxants, para
dissolve the drug. The ability to utilize poorly soluble drugs sympathomimetics, parathyroid calcitonin and
and water soluble stabilizers/excipients offers the ability to biphosphonates, radio-pharmaceuticals, sex hormones (in
form Submicron particles that have high dissolution rates in 50 cluding steroids), anti-allergic agents, stimulants and anorex
aqueous media. The present invention also offers the ability to ics, sympathomimetics, thyroid agents, Vasidilators and Xan
better control the resulting particle size and morphology rela thines. Preferred drug substances include those intended for
tive to techniques described in the above identified prior art. oral administration and intravenous administration. A
Moreover, the present invention often produces particles hav description of these classes of drugs and a listing of species
ing reduced crystallinity as compared to the bulk, unproc 55 within each class can be found in Martindale, The Extra
essed drug, which enhances dissolution. Pharmacopoeia, Twenty-ninth Edition, The Pharmaceutical
Press, London, 1989. More specific examples of drug sub
BRIEF DESCRIPTION OF THE FIGURES stances useful in the practice of the present invention include
but are not limited to danazol, cycloSponine, nifedipine, car
FIG. 1 is a schematic diagram illustrating one embodiment 60 bamazepine, naproxen, triamcinolone and its salts, hydrocor
of the process of the present invention. tisone and its salts, prednisone and its salts, phenylbutaZone,
FIG. 2 is a cross-sectional view of a vessel useful in the betamethasone and its salts, dexamethasone and its salts,
process of the present invention. 17-B estradiol, ketoprofen, Verapamil, ketoconazole, mefe
FIGS. 3-4 are graphs showing improved dissolution rates namic acid, and metronidazole.
for particles of the present invention. 65 The organic solvent into which the drug is dissolved can be
FIG. 5 is an SEM showing reduced crystallinity of the any organic solvent which dissolves the drug to an adequate
particles of the present invention. level. Preferably, the organic solvent dissolves the drug to a
 US 8,551,526 B2
5 6
level of 0.1 weight percent or more, and more preferably to a The drug/organic mixture is sprayed at or below the liquid
level of 1.0 weight percent or more. The organic solvent is level in tank 13 through atomizer 22 to form a jet comprising
advantageously immiscible with water. Suitable organic Sol droplets 23. The jet results in intense mixing between the
vents include diethylether, methylene chloride, ethyl acetate, drug/organic mixture droplets and the aqueous solution.
dimethylether, perfluoroalkanes and isomers thereof, par Thus, as the drug/organic mixture is sprayed through atom
tially fluorinated solvents with or without other functional izer 22, the organic solventis concurrently evaporated into the
groups, and other organic solvents with boiling points below aqueous solution 21 to forman aqueous dispersion of the drug
approximately 70° C., and combinations thereof. particles. In this manner, evaporation of the organic solvent is
In one embodiment, the drug/organic mixture further con occurring rapidly with the spraying and Stabilization of the
tains a particle stabilizer. Stabilization is defined herein to 10 drug particles by the excipients in the aqueous solution.
mean that the resulting drug particles do not grow Substan Evaporation of the organic solvent occurs below the surface
tially, and do not crystallize excessively. In this regard, a of the aqueous solution. An excipient is any Substance com
particle stabilizer is defined herein to mean a substance that bined with an active ingredient to prepare a dosage composi
substantially inhibits particle growth and substantially inhib tion. One example of an excipient is a Surfactant which is a
its crystallization of the drug particles. The particle stabilizer 15 compound that reduces the Surface tension of liquids, or
can be water soluble or organic soluble, although, if the reduces the interfacial tension between two liquids or a liquid
particle stabilizer is water soluble, bioavailability may be and a Solid. Excipients of the present invention may be used
enhanced to an even greater degree. Particle stabilizers can individually or in combination. In addition, excipients may be
also act as absorption enhancers in order to increase bioavail electrostatic or Stearic or any combination of electrostatic and
ability of the drug particles. Stearic.
The particle stabilizer present in the organic can contribute Atomizer 22 can be any device that is capable of breaking
to stabilization of the particle in the aqueous phase. Examples up a bulk liquid into droplets. Suitable devices useful as
of particle stabilizers include phospholipids, Surfactants, atomizers include pressure nozzles, Venturinozzles, vibrating
either low molecular weight or polymeric, Vesicles, poly orifices, ultrasonic spray nozzles, rotating cups or disks,
mers, including copolymers and homopolymers and biopoly 25 bubble caps or grids, or perforated plates.
mers, and/or dispersion aids. The particle stabilizer can be The atomization of the evaporating organic solution into
nonionic, anionic, cationic or Zwitterionic. Suitable Surfac small droplets in the water and the intensity of the spray
tants include gelatin, casein, lecithin, (phosphatides), gum produce intense mixing between the growing drug particles
acacia, cholesterol, tragacanth, Stearic acid, benzalkonium and the water-soluble stabilizers and excipients. The rapid
chloride, calcium Stearate, glycerylinonostearate, cetostearyl 30 evaporation of the organic solvent produces large Supersatu
alcohol, cetomacrogol 1000, polyoxyethylene castor oil ration of the drug and rapid precipitation. The rapid precipi
derivatives, polyoxyethylene sorbitan fatty acid esters, for tation of the drug has the potential to produce amorphous
example, the commercially available Tweens, polyethylene instead of crystalline particles as the time frame is too short
glycols, copolymers of polyethylene glycol and polypropy for crystallization. The hydrophilic stabilizers remain sol
lene glycol, polyoxyethylene Stearates, colloidal silicon diox 35 vated by water during the evaporation of the organic solvent.
ide, phosphates, sodium dodecylsulfate, carboxymethicellu Thus, the stabilizers cover the growing drug particles and
lose calcium, carboxymethylecellulose Sodium, varying the flow rate, nozzle geometry, concentration of drug
methylcellulose, hydroxyethylcellulose, hydroxypropylcel and stabilizer and the nature of the stabilizer(s).
lulose, hydroxypropylmethylcellulose phthalate, noncrystal The temperature of the drug/organic mixture is at a level
line cellulose, magnesium aluminum silicate, triethanola 40 which allows for rapid evaporation of the solvent. Typically,
mine, polyvinylalcohol, sodium lauryl sulfate. (SLS), this temperature will be at least 50 degrees centigrade (C.)
polyvinylpyrrolidone (PVP), bile salts. below the normal boiling point of the organic solvent to 80°
Referring again to FIG. 1, the drug/organic mixture is fed C. above the normal boiling point of the organic solvent. If the
through feed line 12 to a sprayer, where the drug/organic temperature of the drug/organic mixture is at or above its
mixture is sprayed into an aqueous solution contained in tank 45 normal boiling point, feed line 12 must beat sufficient pres
13. The drug/organic mixture is sprayed at or below the liquid Sure to maintain a liquid phase.
level of the aqueous solution in tank 13. The temperature of the aqueous phase is preferably at least
In one alternative embodiment of the present invention, a 10°C., more preferably at least 50° C., and even more pref
portion of the aqueous solution can be sprayed together with erably at least 70°C. The upper temperature limit will depend
the drug/organic mixture into the remaining portion of the 50 upon the operating pressure, but is preferably low enough so
aqueous Solution. In such an embodiment, the nozzle should as not to degrade the drug, but high enough to evaporate the
be designed so as to allow the spraying of two streams simul solvent but not evaporate too much of the water. In a preferred
taneously. In Such an embodiment, the level of the aqueous embodiment, the temperature is less than 120°C., more pref
solution in tank 13 can be controlled by, for example, an erably less than 95°C., and even more preferably less than
overflow, Such that a continuous slurry of particles results. 55 85°C. The pressure of the aqueous solution can be at ambient
The slurry of particles can then undergo further processing to pressure, below ambient pressure to facilitate evaporation or
result in the final drug particles. above ambient pressure.
FIG. 2 is a cross-sectional view of tank 13 containing In the present invention, the drug particles are produced in
aqueous Solution 21. In a preferred embodiment, aqueous a liquid aqueous phase rather than a gas phase. Therefore, the
solution 21 contains at least one particle stabilizer. Suitable 60 particle growth is inhibited by aqueous stabilizers that do not
particle stabilizers include those listed above for inclusion in precipitate. The dissolution rates of the drug particles coated
the drug/organic mixture. The specific particle stabilizer or with water soluble stabilizers may be expected to be high
particle stabilizers selected for use in the aqueous solution 21 since the dispersions come from an aqueous phase. In the
can be the same or can be different from the particle stabili present invention the particle formation stage is distinct from
Zer(s) in the drug/organic mixture. The weight ratio of drug to 65 stage in which the aqueous solution is dried. Therefore the
total particle stabilizer is from 0.01:1 to 10:1, preferably from present invention can provide greater control over particle
0.05:1 to 7:1 and more preferably from 0.1:1 to 4:1. S17C.
 US 8,551,526 B2
7 8
The average particle diameter of the particles in the aque 3:1 or greater, more preferably about 4:1, 5:1, 6:1, 7:1, 8:1,
ous dispersion are from 50 nanometers to 20 microns, more 9:1 or greater, and most preferably about 10:1 or perhaps even
preferably from 100 nanometers to 5 microns, and even more greater.
preferably from 200 nanometers to 1 micron. The drug par In an alternative aspect, the present invention provides
ticles are not necessarily spherical. Average particle diameter poorly water Soluble drug particles that are highly potent,
can be measured using any technique known to those skilled where potency is expressed as a percentage (wt. drug/(wt.
in the art, such as sedimentation field flow fractionation, drug--wt. excipient)). The potent particles of this invention
photon correlation spectroscopy, disk centrifugation or have a potency of greater than about 50%, and perhaps about
dynamic light scattering techniques. 66% or greater, preferably greater than about 70% or 75%,
An advantage of the present invention is the narrow poly 10 more preferably greater than about 80%, 83%, 85% or 87%,
dispersity, also referred to as particle size distribution, that most preferably greater than about 90%, 91%, 92%, 93%,
results. The particle size distribution is typically monomodal, 94%, 95%, 96%, 97%, 98%, 99%, or 100%.
Another aspect of the present invention provides poorly
with narrow size ranges. water Soluble drug particles that possess high Surface area.
As an additional advantage, it is believed that drug particles 15 The surface areas exhibited by particles of this invention are
prepared according to the present invention can exhibit greater than about 2.5 m/g, perhaps even greater than about
reduced crystallinity as compared to the bulk, unprocessed 5 m/g, preferably greater than about 10 m?g, more prefer
drug. Such reduced crystallinity can lead to increased disso ably greater than about 20 m/g, and most preferably greater
lution rates and bioavailability. than about 30 m/g.
The process of the present invention desirably further com The poorly water soluble drug particles of the present
prises the step of recovering the drug particles. In one invention can be amorphous, crystalline or semi-crystalline.
embodiment, recovering the drug particles comprises remov Amorphous meaning primarily amorphous in structure, crys
ing the water from the particles. Removing the water can be talline meaning primarily crystalline in structure and semi
performed using any technique known to those skilled in the crystalline meaning any mixture of amorphous and crystal
art, including spray drying, spray freeze drying, gellation, 25 line domains.
defined as gelling the particles within a polymeric matrix, The disclosed poorly water soluble drug particles can be
lyophilization, drying with cold air, and filtration. produced by any method including solution precipitation,
Advantageously, excipients can be added to either the spray processes, wet milling, mechanical milling, anti-sol
drug/organic mixture or to the aqueous solution, either before vent based precipitation, or other methods in which atomiza
or after the drug particles are formed, in order to enable the 30 tion of drug particles and excipient adsorption are employed.
drug particles to be homogeneously admixed for appropriate While any technique may be utilized, spray freezing or evapo
administration. Suitable excipients include polymers, rative precipitation into an aqueous solution is the preferred
method.
absorption enhancers, solubility enhancing agents, dissolu In another aspect the present invention provides a broad
tion rate enhancing agents, stability enhancing agents, bioad 35 range of liquid dosage form pharmaceutical composition
hesive agents, controlled release agents, flow aids and pro made from the disclosed poorly water soluble drug particles
cessing aids. More particularly, Suitable excipients include including those produced by the methods disclosed herein.
cellulose ethers, acrylic acid polymers, and bile salts. Other Specifically, the present invention includes any of the dis
suitable excipients are described in detail in the Handbook of closed poorly water Soluble drug particle dispersions, com
Pharmaceutical Excipients, published jointly by the Ameri 40 bined with any pharmaceutically appropriate excipients, for
can Pharmaceutical Association and The Pharmaceutical delivery to a Subject. Appropriate pharmaceutical excipients
Society of Great Britain, the Pharmaceutical Press, 1986. include particle stabilizers, tonicity adjusters, buffers, Surfac
Such excipients are commercially available and/or can be tants, mucoadhesive agents, viscosity adjusting agents and
prepared by techniques known in the art. other excipients that are known in the art to prepare disper
An additional embodiment of the present invention 45 sions for pharmaceutical administration. Specific liquid or
involves poorly water soluble drug particles having high dis similar dosage forms that are contemplated include nebuliza
Solution rates; high drug-to-excipient ratios; high potency; or tion, parenteral, topical creams, emulsions, lotions and the
high Surface area. The dissolution rate, according to this like, or transdermal administration forms. Specifically
invention, is the time necessary to achieve a percentage of parenteral administration routes contemplated include dis
particle dissolution at a rate faster than that achieved by the 50 persions administered intraveneously, intramuscularly, Sub
bulk drug under similar conditions, where the bulk drug is cutaneously, intradermally, intrathecally, and may addition
approximately 99% pure without excipients. Dissolution ally comprise buffers, tonicity agents, biodegradable
rates, according to this invention, are greater than about 70%: polymers, preservatives and other excipients that are known
perhaps greater than 80%; preferably greater than 90%; more in the art to prepare dispersions suitable for parenteral admin
preferably greater than 95%; and most preferably 100% of the 55 istration. Moreover, it is contemplated that the dispersions
drug particles dissolved within a period of time 3 times faster may be administered as an oral liquid, and comprise flavoring
than that of the bulk drug. Alternatively such dissolution rates agents, Sweetening agents, bulking agents, buffers, preserva
may be obtained within a period of time about 5 or 7 times tives, tonicity adjusting agents, particle stabilizers, agents to
faster; preferably within a period of about 10 or 15 times modify the Zeta potential and other excipients that are known
faster; more preferably within a period of about 20 or 25 times 60 in the art to prepare dispersions for oral administration. As a
faster; most preferably within a period of 30 times faster; and liquid, no reconstitution is required. In addition, dispersions
perhaps even faster when compared to that of the bulk drug. according to the invention may be formulated for administra
Exemplary dissolution profiles are depicted at FIGS. 13(a)- tion topically to the eye to treat Surface or intraocular condi
(c). tions, and may comprise buffers, preservatives, tonicity
The poorly water soluble drug particles of the present 65 adjusting agents, particle stabilizers, viscosity modifiers and
invention can possess a drug-to-excipient ratio of about 2:1, other excipients that are known in the art to prepare disper
although it is preferable for the drug-to-excipient ratio to be sions for application to the eye. Also, the dispersions contem
 US 8,551,526 B2
10
plated herein may be formulated for administration topically used as the particle stabilizer. The drug/organic mixture was
to the skin, Surface of the eye, ear, nasally, vaginally or rec sprayed into 10 mL of aqueous solution at a rate of 1 ml/min.
tally as an ointment, cream or gel, and may comprise buffers, Table A lists processing parameters and the resulting particle
preservatives, tonicity adjusting agents, particle stabilizers, sizes.
Viscosity modifiers and other excipients that are known in the
art to prepare dispersions for application to the area. It is TABLE A
further contemplated that the dispersion may be formulated
for administration in a transdermal patch comprising adding Drug
the dispersion with polymers, gelling agents, absorption organic Aqueous Spray Tween-80 Median percent
enhancing agents, particle stabilizers, adhesive agents and 10
temp. temp time conc (wt particle particles
other excipients Ex (° C.) (° C.) (min) percent) size (nm) <median size
While the invention is described herein primarily in con
nection with its preferred utility, i.e., with respect to micro 1 65 55 10 1 470 11
and nanoparticulate drug Substances for use in pharmaceuti 2 65 55 10 1 608 64
cal compositions, it is also believed to be useful in other 15
3 65 65 10 1 1114 61
applications such as the formulation of particulate cosmetic 4 65 65 10 1 759 41
compositions and the preparation of particulate dispersions 5 70 65 10 1 706 33
for use in image and magnetic recording elements.
The following examples are for illustrative purposes only 6 70 65 10 1 796 43

and are not intended to limit the scope of the claimed inven 7 70 65 10 1 932 50
tion. Percentages are in weight percents unless otherwise 8 70 65 2O 5 322 14
stated.
EXAMPLES
25
Examples 9-13
For the following examples, the apparatus shown in FIG. 1
is used. The drug/organic mixture was fed via a Constametric The drug was cyclosporine, the organic was diethylether,
3200 HPLC pump through a preheating coil into a 30 mL
receiving tank containing the required amount of aqueous and the concentration of the drug/organic mixture was as
Solution. The nozzle used for the spraying was made by 30 shown below in Table B. For the aqueous solution, phosphati
cutting/16" stainless steel tubing to form an elliptical conical dylcholine (10 wit percent), a Sigma egg lecithin, 60 percent
geometry at the end. The end of the tube was filed to obtain the pure, was a surfactant, or other excipient, used as a particle
desired flow rate. Nitrogen was continuously flowed down stabilizer. The drug/organic mixture was sprayed into 10 mL
ward to break up foam in cases where it formed. For all of the aqueous solution at a rate of 1 ml/min. The temperature of the
examples, particle size was measured by dynamic light scat 35 aqueous solution is 75° C., while the drug/organic mixture
tering techniques within 4 hours of the spray. was sprayed into the aqueous solution at a temperature of 75°
Dissolution testing for the following examples was carried C. Table B lists some processing parameters and the resulting
out using a Vankel dissolution apparatus following the USP particle sizes.
Apparatus II paddle method. During all dissolution tests, to
ensure sink conditions, only 10-30 percent of the saturation 40
TABLE B
solubility of the drug was added to the dissolution apparatus.
The appropriate amount of final drug preparation was Drug conc Particle
weighed and added to 900 ml of distilled water. Each sample Drug conc in Spray in aqueous Drug size
organic solin time (mg/ml Surfactant range
was stirred at 50 rpm using a paddle-type stirrer. The disso EX (wt percent) (min) water) ratio (nm)
lution apparatus was maintained at 37° C. throughout the 45
experiment. Samples in the amount of 5 ml were automati 9 1 2O 14.5 O.13 135-390
10 2 19 30.8 O.28 120-575
cally withdrawn at 10, 20, 30 and 60 minute intervals. These 11 5 10 37.1 O.33 90-300
samples were filtered using a 0.45 um filter (Gelman OHP 12 5 10 34.9 O.32 215-590
Acrodisc 0.45 um, VWR). To ensure that no precipitation 13 10 6 29.7 O.30 170
occurred during HPLC analysis, 0.5 ml of organic solvent 50
was added to 3 ml offiltered sample. This organic solvent was
preferably the organic component in mobile phase (acetoni
trile). These were mixed using a Vortex mixer at high speed Examples 14-16
for approximately 10 seconds and then refiltered using a 0.45
um filters into a HPLC vial for analysis. HPLC analysis was 55
The drug was cyclosporune (5 wt percent), the organic
different for each drug and the exact methods being modified solvent was that listed in Table C below. For the aqueous
from those suggested in HPLC methods for pharmaceutical solution, Poloxamer 407(1 wtpercent), also known as Lutrol
analysis by George Lunn and Norman R. Schmuff, John F127, a poly(ethylene)-poly(propylene) block polymer con
Wiley & Sons, NY, 1997. sisting of 73 percent of polyethylene glycol and 27 percent
60
Examples 1-8 polypropylene glycol with an average molecular weight of
12,000 (BASF), was a surfactant, or other excipient, used as
The drug was cyclosporine, the organic was diethylether, a particle stabilizer. The drug/organic mixture was sprayed
and the concentration of the drug/organic mixture was 5.0 into 25 mL aqueous solution at a rate of 1 ml/min. The
weight percent cyclosporine in diethylether. For the aqueous 65 temperatures of the aqueous solution and of the drug/organic
solution, Tween-80, a polyoxyethylene sorbitan monolaurate mixture were 75°C. Table C lists some processing parameters
(ACROS) was a surfactant, or other excipient, which was and the resulting particle sizes.
 US 8,551,526 B2
11 12
TABLE C dish and vacuum dried for at least 10 hours at temperatures
ranging from 40-60° C. and a vacuum level of 30 inches of
Drug conc in Hg. The resulting Solids were mechanically ground to a pow
aqueous (mg/ml Drug surfactant Particle size der and dissolution studies were performed on these powders.
Ex Organic Solvent water) ratio range (nm)
5 The results of these dissolution tests were compared with that
4 Diethyl Ether 15 1.5 320-1000 for bulk TAA. The results shown in FIG. 3 indicate the
15 Dichloromethane 17.8 1.78 160-345
16 Dichloromethane 14.8 148 196-2O2 increased dissolution rates of TAA processed according to the
present invention.
10 TABLE F
Examples 17-21
Organic Amount of HPMC added for
The drug was danazol, and the solvent was methylene Ex stabilizer Aqueous stabilizer gellation (g)
chloride. The particle stabilizer in the aqueous solution is 7 PVP K-15 Deoxycholic acid 3
listed below in Table D. In all cases, the concentration of the 15 28 Poloxamer 407 PVP K-15 2
particle stabilizer in aqueous Solution was 1 weight percent. 29 Poloxamer 407 Deoxycholic acid 2
The drug/organic mixture (2 wit percent drug) was sprayed
into the aqueous solution at a rate of 2 ml/minute for 5 min
utes. The temperature of both the aqueous solution and the Examples 30-32
drug/organic mixture was 75°C. The drug/excipient ratio was
1.06. The drug was carbamazepine and the solvent was methyl
ene chloride, The temperature of the drug/organic mixture
TABLED and the receiving aqueous solution was 87°C. The concen
Ex Particle stabilizer Particle size range (nm)
tration of drug in the organic was 1.0 weight percent. The
25 particle stabilizers in the aqueous solution are listed in Table
17 Sodium lauryl Sulfate 370-415 G. In all cases the concentration of the particle stabilizer in the
18
19
Poly (vinyl pyrollidone)
Poly (vinyl pyrollidone)
140-28O
315-450
aqueous Solution was 2 weight percent and the organic solu
2O Poloxamer >1000 tion contains, in addition to the drug, 0.5 weight percent
21 *Myri 52 >1000 Poloxamer 407. The volume of the aqueous solution was 20
30 ml. In all cases the resulting aqueous drug Suspension was
*Myris polyoxyethylene monostearate sprayed into liquid nitrogen and the frozen particles were then
lyophilized for 24 hours. The resulting powder was thor
Examples 22-26 oughly mixed and dissolution studies were performed on
these powders. The results of these dissolution tests were
The drug was Carbamazepune, and the solvent was meth 35 compared with those for bulk carbamazepine. The results
ylene chloride. The concentration of drug in the organic was shown in FIG. 4 clearly indicate the increased dissolution
2 weight percent. The particle stabilizer in the aqueous solu rates of carbamazepine processed according to the present
tion is listed below in Table E. In all cases, the concentration invention over the bulk unprocessed carbamazepine. The
of the particle stabilizer in aqueous solution was 1 weight crystallinity of these powders was also studied, with the result
percent. The drug/organic mixture was sprayed into the aque 40 being a reduction in crystallinity as compared to the bulk
ous solution at a rate of 2.5 ml/min. The temperature of both drug.
the aqueous solution and the drug/organic mixture was 75°C. TABLE G
The drug/excipient ratio was 1:30.
45 Ex Aqueous stabilizer
TABLE E
30 Deoxycholic acid
Ex Particle stabilizer Particle size range (nm) 31 PVPK-15
32 SLS
22 Sodium lauryl Sulfate (SLS) >7000
23 Poly (vinyl pyrollidone) (PVP) 320-1000
24 Polyethylene glycol 290-SSO 50
25 Poloxamer >1000 Example 33
26 Myri 52 >1000
The drug was carbamazepine and the solvent was methyl
ene chloride. The temperature of the drug/organic mixture
Examples 27-29 55 and the receiving aqueous solution was 87°C. The concen
tration of drug in the organic was 1.0 weight percent. The
The drug was Triamcinolone acetonide, also referred to particle stabilizer in the aqueous solution was 2 weight per
herein as TAA, and the solvent was methylene chloride. The cent deoxycholic acid and that in the organic Solution was 5
concentration of drug in the organic was 0.5 weight percent. weight percent Poloxamer 407. The organic solution was
The particle stabilizers in the aqueous solution and the 60 sprayed at 2 ml/min for 27 minutes into 50 ml of the aqueous
organic Solution are listed in Table F. In all cases the concen deoxycholic acid solution. The Suspension was immediately
tration of the particle stabilizer in the aqueous solution was 1 spray dried in a Buchi 190 spray dryer where an inlet tem
Weight percent and in the organic solution was 0.5 weight perature of 145-150 degrees C. and an outlet temperature of
percent. The volume of the aqueous Solution was 15 ml. In all 90-95°C. were maintained. The resulting dry powder was
cases the resulting aqueous drug Suspension was poured into 65 collected, and an SEM micrograph of this powder is shown in
a Hydroxypropylmethyl cellulose (HPMC) (grade E-5), thor FIG. 5. The Figure shows no crystalline particles indicating
oughly mixed by hand, poured into a Glass crystallization the amorphous nature of the drug produced using EPAS.
 US 8,551,526 B2
13 14
Examples 34-37 other excipient, in order to raise the potency in the precipitate.
The adsorbed surfactant, or other excipient, was sufficient to
The drug was nifedipine and the solvent was methylene prevent aggregation and enhance wetting to maintain a high
chloride. The concentration of drug in the organic was 1.0 Surface area and likely a high local equilibrium concentration
weight percent. In all cases the stabilizer in the aqueous of API in the diffusion layer. The dissolution rate was ana
solution was poly(vinyl alcohol) (PVA). The volume of the lyzed as a function of the Surfactant, or other excipient,
aqueous solution was 20 ml. Table H lists excipients added to adsorption, particle size, Surface area, contact angle, particle
the aqueous solution in addition to the PVA. In all cases the morphology and crystallinity.
resulting aqueous drug Suspension was rapidly frozen by Materials
dipping the sample container in liquid nitrogen and then 10
Danazol was purchased from Spectrum Chemicals &
lyophilized for 24 hours. The resulting powder was thor Laboratory Products Corporation (Catil D1103). Pluronic
oughly mixed and dissolution studies were performed on F127 (BASF), Polyvinylpyrrolidone (PVP K-15, Mw =15,
these powders. The results of these dissolution tests were 000 and PVP 40T, Mw-40,000) (Sigma, St. Louis, Mo.),
compared with that for bulknifedipine. The results, shown in
FIG. 6, clearly indicate the increased dissolution rates of 15 Sodium dodecyl sulfate (Sigma) and Deoxycholic acid
EPAS processed nifedipine over the bulk unprocessed nife (Sigma) were used as received. HPLC grade acetonitrile was
dipine. The crystallinity of these powders was also studied from Merck (Germany) and spectro grade dichloromethane
using X-ray diffraction patterns, with the Result being a was from Fisher Scientific Co. (NJ, USA)
reduction in crystallinity of the drug processed according to Evaporative Precipitation into Aqueous Solution (EPAS)
the present invention AS compared to the bulk drug. The organic danazol solution was fed by an HPLC pump
through a 3 m long /16 in. o.d.x0.030 in. i.d. stainless steel
TABLE H coiled tube contained within a 1/2" ODx24" long plastic
Excipients in aqueous
water jacket (Alltech). Water was circulated through the
Ex solution jacket with a JULABO MP temperature controller. The
25 organic solution was atomized through an unheated insulated
34
35
1.5 wt percent PVP K40
1.5 wt percent SLS
adjustable restrictor (5 mm dia.x136 mm long, ISCO, USA)
36 1 wit percent Poloxamer 407 into hot water. Atomization was achieved by adjusting the
37 1 wit percent PVP K15 nozzle valve manually to maintain a pressure drop to about
3500 psi. The aqueous stabilizing Solution was contained in a
30 250 ml plastic submerged in a temperature-controlled water
Examples 38-39 bath. The nozzle was submerged approximately 10 cm under
the surface of the aqueous solution. To suppress and drain the
foam produced by the organic vapor, nitrogen was blown
The drug was ketoprofen and the solvent was methylene downwards on top of the foam at 20 psi into the cylinder
chloride. The temperature of the sprayed drug/organic mix 35 through three /16 in. o.d.x0.030 in. i.d. stainless steel tubes.
ture and the receiving aqueous solution was 87°C. The con Unless indicated otherwise, the stabilizer was added in the
centration of drug in the organic was 1.0 weight percent. The aqueous phase and was not present in the organic feed solu
particle stabilizers in the aqueous solution are listed in Table tion. After spraying for a required time to produce the desired
3. In all cases the concentration of the particle stabilizer in the drug/excipient ratio, the Suspension was recovered and ana
aqueous Solution was 2 weight percent and the organic solu 40 lyzed within 30 mins to determine the particle size by light
tion contains, in addition to the drug, 0.5 weight percent scattering with a Malvern Mastersizer-S (Malvern Instru
Poloxamer 407. The volume of the aqueous solution was 20 ments Ltd., U.K.).
ml. In all cases the resulting aqueous drug Suspension was Excipient Adsorption Measurement
rapidly frozen by dipping the sample container in liquid nitro To quantify excipient stabilization of the danazol particles
gen and then lyophilized for 24 hours. Crystallinity studies 45 in the EPAS Suspension, excipient adsorption was measured
were performed on these powders using X-ray diffraction based on a mass balance between the Supernatant and pre
patterns, and were compared with that for bulk ketoprofen, cipitate. In these measurements, W was the weight of the
which resulted in the processed powder exhibiting amor Supernatant before drying, which includes the weight of
phous character as opposed to the bulk ketoprofen. water, excipient and danazol, which may dissolve in micelles
TABLEJ
50 or excipient complexes if formed. W was the weight of the
Supernatant after drying, thus (W-W) was the amount of
Ex Aqueous stabilizer water in the supernatant. W, was the weight of the precipi
tate before drying, which includes danazol, adsorbed excipi
38 Deoxycholic acid ent and a Small amount of Supernatant with the same compo
39 SLS 55 sition as the bulk Supernatant. W, was the weight of the
precipitate after drying. W., was the amount of danazol in
the precipitate measured by HPLC. W., was the amount of
Examples 40-45 adsorbed excipient on danazol. Since composition of the
Small amount of supernatant in the precipitate was assumed to
Danazol particles with high dissolution rates and 60 be the same as that in the bulk Supernatant
extremely high drug:excipient ratios greater than about 5.
corresponding to a potency (wt drug/wt drug--wit excipient)
above 80% were produced by EPAS. An aqueous suspension
was produced by EPAS to produce surfactant, or other excipi Wed Wodan Wpsuf (1)
ent, coated particles with a low drug:excipient ratio ranging 65 W - Wed
from 1:4 to 1:1. The suspension was then centrifuged and the
Supernatant was decanted to remove the free Surfactant, or
 US 8,551,526 B2
15 16
From this equation, the amount of adsorbed excipient on through 0.45 um Syringe filters and 2 ml of each sample were
danazol was given by diluted with 0.1 ml acetonitrile before analysis. Danazolcon
centrations were measured using HPLC (SHIMADZU,
LC-600, Japan).
W ) (2) Particle Size
Walt = Wi-Wan - (Wa-W4)x(ww. S 's Particle size distributions, based on volume fraction, of the
original EPAS suspension and redispersed dry powder were
measured by static light scattering with a Malvern Master
To measure the amount of excipient adsorbed on the par sizer-S. To measure the particle size distribution, 5 ml sus
ticles, 1% w/v danazol solution in dichloromethane was 10 pension with 5 mg drug/ml water concentration, was diluted
sprayed into 15 ml aqueous solution containing 1% w/v. with 500 ml distilled water, to produce a light obscuration in
excipient at a flow rate of 1 ml/min for 7.5 mins to produce a the range of 10-30% for accurate measurement. To study the
suspension with a drug to excipient ratio of 0.5:1. The pres redispersibility of the dry powders after centrifugation and
sure drop was 3000-4000 psi and the temperature was 75°C. vacuum drying, about 50 mg dry powder were Suspended into
After centrifugation, the Supernatant and the precipitate were 15 500 ml distilled water to produce an obscuration in the range
weighed before and after drying at 55° C. and -30 in. Hg. 10-30%. After 1 minute, the particle size distribution was
High Potency Danazol Powder by Centrifugation measured. In a control experiment, bulk danazol was dis
Two percent (2%) w/v danazol solution in dichlo persed in 500 ml 0.02% non micelle-forming PVP 40Taque
romethane was sprayed at a flow rate of 1 ml/min into 100 ml ous solution, since it was very hydrophobic and difficult to
aqueous solution containing 1% w/v excipient or a excipient disperse in pure water. Ultrasound was used in the measure
mixture at 1:1 w/w ratio, if two surfactants were used, to ment to break up the agglomerated particles.
stabilize the drug particles. The temperatures of both heating Contact Angle
jacket and water bath were 80° C. and the pressure drop was mg dry powder was filled into a 0.7 cm diameter flat faced
3500-4000 psi. After 25 minutes spray, a suspension with die and compressed with a Carver Laboratory Press (Model
drug to excipient ratio of 0.5 was recovered and the particle 25 M, Fred S. Carver Inc, WIS, USA) at 1500 kgfinto a tablet. A
size of the danazol particles was measured with Malvern drop of 51 ul distilled water was placed on the surface of the
Mastersizer-S. The suspensions were centrifuged (BECK tablet and contact angle was measured from the tangential
MAN, Model TJ-6, USA) at 3000 rpm for 30 mins. The angle of the water drop with help of a camera (Panasonic
Supernatants were poured out and the precipitates were WV-1410, Philippines).
placed into a vacuum oven and dried at 40°C., and -30 inHg 30 Stressed Cycle Stability Study
for 3-4 hrs. The crystallinity of the dry powders was examined Dry powders were placed in 60 ml Qorpak R. glass bottles,
by X-ray diffraction (PW1720, PHILIPS). The surface area of sealed with sodium calcium aluminosilicate hydrate desic
the dry powders was measured with a high-speed Surface area cant containing cobaltous chloride indicator (VWR Interna
BET analyzer (NOVA 2000, Quantachrome Instruments, tional, West Chester, Pa.). The temperature cycle was:
USA). 35 increase temperature from -5°C. to 40°C. over 30 mins, hold
Dissolution Test at 40° C. for 2.5 hours and then decrease temperature from
After centrifugation and vacuum drying, 20 mg dry powder 40° C. to -5°C. over 30 mins. The cycle was repeated 6 times
was placed into a USP basket assembly and stirred at 50 rpm per day. The humidity was dry and the duration of the stability
in pH 9.0 SDS/tris buffer, which contained 0.75 w/v % study was 2 weeks. The characteristics of the dry powders
sodium dodecyl sulfate and 1.21 w/v '% tris (hydroxymethyl) 40 were studied over two weeks.
aminomethane PD 2960 in aqueous solution for 1 hour. The Results and Discussion
stirring rate was then increased to 200 rpm for 1 hour. Ali Excipient Adsorption Study
quots of the dissolution medium (5 ml) were sampled at 2, 5. The adsorption of various Surfactants onto drug particle
10, 20, 30, 60 and 120 mins. The aliquots were filtered surfaces during EPAS are listed in Table K(1).
TABLE K(1)
Adsorption of excipient onto danazol in EPAS Suspension
Aqueous M of W/W,
excipient Properties Chemical structure of excipients excipients (m/m,96)
PVP K-15 Homopolymer
U 15,000 13.O 2.43
N O

—i-cis pi

PVP4OT Homopolymer 40,000 1.O.O. 1.01

Pluronic Copolymer HO(CH2CH2O)98(CH2CHO)67(CH2CH2O)98H 12,528 3.87 - 1.43

F127
hi,
Pluronic Copolymer 12,528 11.2 - 0.72
F1278
 US 8,551,526 B2
17
TABLE K(1)-continued
Adsorption of excipient onto danazol in EPAS suspension

Aqueous M of W/W,
excipient Properties Chemical structure of excipients excipients (m/m,96)
DCA Anionic CO2H 414 5.79 - 1.61
Surfactant

SLS Anionic CH(CH2)CH-O-SO-ONa 288 5.44 - 0.46

Surfactant

Adsorption measurement after 3 days storage at ambient conditions,

TABLE K(2) TABLEM

Pluronic F127 adsorption on danazol particles after 3 days storage Concentration of danazol in the Supernatant, recovery
25
from the precipitate and its potency (g danazolig powder)
West. in the dry powders
W W. W. W. Wedan West. Weian
(g) (g) (g) (g) (mg) (mg) (%) Potency of
Cas Danazol recovery danazol
1.8987 0.0414 O.1276 O.O2OO 1S.820 1888 11.9 Aqueous excipient (mg/ml) (%) (%)
1.5594 O.O373 O.O901 O.O213 17.753 1862 1O.S
30 PVP K-15 O.OOO2 100 88.5
PVP4OT O.OOO1 100 92.3
Table M shows the concentration of danazol in the Super Pluronic F127
DCA
0.035
O.O84
99.3
98.3
89.3
85.1
natant. For PVP 40T and PVP K-15, the concentration of SLS O.804 82.1 83.2
danazol in the Supernatant solution was on the order of the PVP4OT - Pluronic F127 O.OO9 99.8 91.5
detection limit which was 0.02 g/ml. The fraction of danazol 35 PVP4OT - DCA O.O2O 99.6 86.4
in the aqueous Suspension recovered in the precipitate after PVP4OT - SLS O.191 96.2 92.9
centrifugation was above 99%. For Pluronic F127, SDS and
DCA, the recoveries decreased, but were still greater than Dissolution Rate
96.2% for each excipient except for SDS. After centrifugation
and vacuum drying, the potency of danazol in the dry powders 40
As shown in FIGS. 9(a) and 9(b), the dissolution rate was
was higher than 83.2%, as shown in Table L. Drug:excipients much higher for PVP K-15, PVP4OT or PVP40T+SDS than
ratios varied from 4:1 to 9:1. the other stabilizers. In two mins, 70, 80 and 90% danazol was
TABLEL dissolved with PVP4OT, PVP K-15 or PVP4OT--SDS as the
Surfactants, respectively. For the other systems, the dissolu
Particle size of danazol in the Suspension at excipient 45
tion rates were much lower, closer to that of bulk danazol. We
concentration was 1% WV and its redispersibility after drying. will show below that these systems had larger particle sizes
D (v, 0.5) and lower Surface areas.
D (v, 0.5) D (v, 0.5) (Lm) The effect of adsorbed excipient and free excipient on
(Lm) (Lm) redispersed dissolution rate was studied by mixing PVP 40T precipitate
EPAS Suspension dry powders
Aqueous Excipients Suspension with ultrasonic woultrasonic 50 from the centrifuged EPAS suspension with PVP 40T powder
to form an overall drug to excipient ratio of 0.5. As shown in
Bulk Danazol 29.63
21.07 (30s)
FIG. 9(a), the dissolution rate did not change. The changes in
PVP K-15 29.47 15.27 (15s) 14.15 Surface area, diffusion layer thickness and concentration of
12.50 (30s) 7.60 (30s) the API in bulk solution from the EPAS spray and adsorbed
PVP4OT 49.28 13.82 (15s) 14.07 55 excipient were sufficient to produce high dissolution rates,
17.62 (30s) 10.53 (30s) without any need for mixing in additional stabilizer powder.
PVP4OT - SLS 16.8O 13.82 (30s) 18.00
12.13 (30s) Particle Size Distribution and Redispersibility of the Dry
Pluronic F127 80.35 32.29 (15s) 39.73 Powders
25.09 (30s) 22.17 (30s) The mean particle sizes of the EPAS suspensions, EPAS
DCA 100.09 24.64 (30s) 56.86
23.88 (30s)
60 Suspensions after Sonication, and redispersed dry powders
SLS 70.62 31.65 (15s) 61.14 after centrifugation and vacuum drying are shown in Table L.
27.50 (30s) 29.32 (30s) The particle sizes, both with and without sonication, are cor
PVP4OT - Pronic F127 125.92 28.75 (30s) 71.73 related with the adsorption during the EPAS spray given in
26.16 (30s) Table K.
PVP4OT - DCA 121.77 28.02 (15s) 52.90
23.61 (30s) 23.23 (30s) 65 X-Ray Diffraction
X-ray diffraction was used to analyze the crystallinity of
the dry powders. As shown in FIG. 9, the crystallinity of
 US 8,551,526 B2
19
danazol was lower for the vacuum dried precipitates from TABLE P
EPAS relatively to bulk danazol. The a-peak heights of dana
Zol in different excipient systems at 20=15° are listed in Table Contact angle of dry powder after centrifugation and drying
N. The reduction in crystallinity was less than 20% after Excipient Contact angle ()
correction for the presence of 10% w/w excipient. It was 5
Bulk danazol 61.5 61.O
assumed that the danazol peak height was linear in concen PVP K-15 4.1.8 40.4
tration for a fixed weight. The degree of crystallinity for these PVP4OT 48.8 47.0
samples did not appear to be correlated to the particle size or Pluronic F127 34.0 34.0
DCA 19.9 17.8
dissolution rates. Thus enhanced dissolution rates are pos 10 SLS 7.0
sible even with only a modest reduction in crystallinity. PVP4OT - Pronic F127 42.O 37.5
PVP4OT - DCA 34.0 36.2
TABLE N PVP4OT - SLS 14.6 13.2

The peak height of danazol x-ray diffraction at 20 = 15° 15 Cyclic Stability Study
Two week cyclic stability tests were undertaken under
Excipient Peak height (counts) harsh storage conditions for the three systems with the high
Bulk danazol 3182
est dissolution rates. Samples were analyzed each week to
determine if the potency, particle size, crystallinity, dissolu
PVP K-15 2358 tion rate and morphology had changed with time. The con
PVP4OT 1942 centrations of danazol in the three systems were: 88.9% with
Pluronic F127 2843 SD (standard deviation) of 2.9% in PVP K-15+Danazol,
DCA 2413 93.6% with SD of 1.4% in PVP4OT.-Danazoland 89.6% with
SLS 2867 SD of 5.0% in PVP4OT-SDS--DanaZO1.
PVP4OT - Pluronic F127 2S46 25 Redispersibility of the Dry Powder
PVP4OT - DCA 2371 The dry powders were redispersed into 500 ml pure water.
PVP4OT - SLS 2465 Changes over two weeks are shown in FIG. 10. Without
ultrasound, the size of particles stabilized with PVP K-15
increased from 9.7 um to 25.5 um after two weeks. However,
Surface Area 30 after 15 seconds Sonication, the primary particle size
The BET surface areas of the dry powders were analyzed. decreased to 8 um for both samples. For the PVP K-15 sys
As shown in Table O, systems with small particle size and tem, agglomeration of the dry particles increased with time.
These agglomerates were broken into primary particles with
high dissolution rates, that is danazol with PVP K-15, PVP ultrasound. The moisture in the container was minimal due to
40T or PVP 40T+SDS, had surface areas on the order of 5 desiccant.
m?g. 35
X-Ray Diffraction
X-ray diffraction was used to study the crystallinity of the
TABLE O dry powders. As shown in FIG. 11 shows the diffraction
Surface area of the dry powder profiles of danazol over 2 weeks.
40 Surface Area
Excipient Surface Area (m?g) FIG. 12 shows the surface area of danazol systems over
Bulk danazol O.S2 time. This result was in accord with the stability of the drug
PVP K-15 5.55 particle size over time. FIG. 14 shows that danazol with PVP
PVP4OT 4.89 40T+SLS has a smooth crystal surface, but with PVP K-15 or
PVP4OT - SLS
Pluronic F127
4.98
3.13
45 PVP 40T it has a fluffy Surface, despite the similar crystal
DCA 3.72
linities.
SLS 3.07 Dissolution Rates
PVP4OT - Pluronic F127 3.28 The dissolution results are shown in FIG. 13. The dissolu
PVP4OT - DCA 3.22 tion rate did not change over time, nor did other certain
50 properties of these drug powders, including the particle size
and surface area. For the two week cyclic stability study, high
Contact Angle potency danazol dry powders with PVP K-15, PVP 40T or
The contact angle results are shown in Table P. For systems PVP 40T and SDS as stabilizing excipients were very stable
with high dissolution rates, contact angles were close to the when desiccant was used to prevent to the particles from the
value of pure PVP which was 43, indicating high surface 55 moisture.
coverage by PVP. For the anionic excipient systems, the con What is claimed is:
tact angles were very low. The overall contact angle may be 1. A method of producing poorly water Soluble drug par
written as ticles for release comprising the steps of
providing a drug;
cos 0 if cos 0-fcos 02 60 providing a container comprising aqueous Solution;
spraying the drug and one or more excipients below the Sur
wheref, and f, are the fractions of the surface occupied by face level of the aqueous solution wherein the one or more
Surface types having contact angles 0 and 0. The con excipients selected from polyoxyethylene Sorbitan monolau
tactangles in Table Pare below the values expected from rate, phosphatidylcholine, a poly(ethylene)-poly(propylene)
this equation, based on the pure component values 0 65 copolymer, sodium lauryl sulfate (SLS), Poly(vinyl pyrroli
and 0, indicating that the Surface was enriched by the done) (PVP), Poloxamer, polyoxyethylene monostearate,
hydrophilic excipient. gelation agent, deoxycholic acid, poly(vinyl alcohol) (PVA).
 US 8,551,526 B2
21 22
cetostearyl alcohol, methylcellulose, hydroxyethylcellulose,
hydroxypropylcellulose, hydroxypropylmethylcellulose
phthalate, noncrystalline cellulose, magnesium aluminum
silicate, and triethanolamine;
forming one or more stabilized drug particles by Solution
precipitation, anti-solvent precipitation, spray freezing,
evaporative precipitation or lyophilization;
separating said one or more stabilized drug particles from
a Suspension solution;
removing said solution from the one or more stabilized 10
drug particles; and
producing one or more stabilized drug particles having a
drug-to-excipient ratio of greater than about 4:1 and an
average particle diameter from 50 nanometers to about
20 microns; and 15
a dissolution rate greater than about 65% drug in about 60
minutes;
wherein the drug-to-excipient ratio is about 2:1, 3:1, 4:1,
5:1, 6:1, 7:1, 8:1, 9:1, 10:1 or greater;
wherein the drug particles have a surface area greater than
about 2.5 m/g, 5 m/g, 10 m/g, 20 m/g or 30 m/g; and
wherein the drug potency is about 80% or 100%.
2. The method of claim 1, wherein the drug particles are
separated by centrifugation, settling, or filtering.
3. The method of claim 1, wherein the step of removing the 25
Solution from the resulting drug particles comprises lyo
philization, vacuum dried, or spray drying, or spray drying.
4. The method of claim 1, wherein the amount of drug
dissolved is about 80%, 85%, 90%, 95% or 100%.
5. The method of claim 4, wherein the dissolution occurs 30
about 5, 7, 10, 15, 20, 25 or 30 times faster than the bulk drug.
k k k k k