article_1680257103
article_1680257103
article_1680257103
922
Review Article
Sonpal et al. WORLD JOURNAL OF PHARMACEUTICAL
World Journal of Pharmaceutical and Medical Research
AND MEDICAL RESEARCH ISSN 2455-3301
www.wjpmr.com Wjpmr
Sonpal Singh Thakur*, Dr. Jagdish Rathi, Karan Rajak, Kripal Gurjar, Madiha Khan, Mahendra Kumar
Sharma and Mahendra Kumar Thakur
NRI Institute of Pharmaceutical Sciences, Sajjan Singh Nagar, Opposite Patel Nagar, Raisen Road Bhopal, MP,
462022.
ABSTRACT
Plants serve as a rich source of bioactive molecules, which are used to treat various diseases in Ayurveda.
Medicinal plant materials are formulated into valuable Ayurvedic medicines by application of modern scientific
techniques, where standardization plays a pivotal role for authentication. Standardization confirms the identity,
quality and purity of drugs. World Health Organization has set up suitable specific standardization parameters to
evaluate the crude drugs and their finished products. These include various evaluation techniques such as
pharmacognostical, physico-chemical, phytochemical, analytical, biological and biotechnological. Nowadays,
application of several modern analytical techniques has become inevitable for evaluating the polyherbal Ayurvedic
formulations to ensure quality, safety and efficacy. Various spectroscopic and chromatographic methods applicable
for this purpose are ultra-violet spectroscopy, Fourier-transform infrared spectroscopy, nuclear magnetic resonance
spectroscopy, thin-layer chromatography, high performance thin layer chromatography, high performance liquid
chromatography, gas chromatography, mass spectroscopy and hyphenated techniques such as gas chromatography-
mass spectroscopy, liquid chromatography-mass spectroscopy, liquid chromatography-nuclear magnetic resonance
spectroscopy. Out of several formulations available in Ayurveda, asavas and aristas are considered as unique
dosage forms due to their indefinite shelf life. Standardization and formulation of different asava-arista
formulations using various analytical techniques are vividly discussed in this review.
Method DISCUSSION
Wash, dry and powder the herbal components and pass
An attempt has been made to review and understand the
each of them seperately through sieve number 44 to get a
asava – arishta, a dosage form from the classical,
coarse powder.Boil haritaki powder in the required
pharmaceutical and standardization perspective. A
quantity of water till it reduces to ¼ of its initial
review of the available literature suggests that the
quantity.Screen the mixture by passing it through a clean
industrial approach for the preparation of fermented
muslin cloth to get rid of the impurities and the residual
preparations, asava–arishta are based on traditional
herb part. Add jaggery, sugar and honey to the clear
principles.The new approaches with new techniques
decoction and keep stirring till everything mixes properly
contribute to better quality control for the large scale
next, pour the decoction into a wide-mouthed vessel
production. It must however be noted that the asava-
lubricated with ghee from the inside. Add aloe vera gel
arishta preparations produced adopting modern
and the remaining powdered herbs to the vessel.Lock the
parameters of standardization as against by traditional
mouth of the container with a mud-smeared cloth tightly.
method may pose some limitations. The limitations in
Keep the container untouched in the fermentation room
case of asava-arishta standardization arise at all three
and allow it to ferment for a month. On culmination of
steps of raw material standardization, process
the fermentation process, screen the fermented liquid
standardization and finished product standardization. In
through a clean muslin cloth to abolish solid particles
case of raw material: Relevance of madhura dravyas i.e.
and impurities. Pour the herbal concoction into an
sweeteners like sugar, honey or jaggery to a particular
amber-coloured, air-tight glass jar. Keep the jar in a cool,
ingredient or group of ingredients; proportion to which it
dry environment for maturation.
is used and time of addition will definitely affect the
alcoholic extraction of therapeutic attributes during
Standardisation
fermentation. These are required to be critically and
Dasamularista
comparatively studied. W. fruticosa, M. longifolia,
In a comparative study, Dasamularista was prepared
Surabeeja or Kinva are added in liquid for fermentation.
using identical size, shape and capacity of earthen pots,
Among these the most beneficial trigger medium for
stainless steel vessel and porcelain jar by filling up to ½,
fermentation is to be examined. Use of yeast as a reliable
2/3rd and 3/4th capacity of the container. TLC using
medium to trigger and enhance fermentation process is
solvent system butanol, acetic acid and water (63:17:10)
known; however, its comparative effect as against
showed five spots in different preparations. From
Dhataki flowers are yet to be established for quality and
different analytical and physico-chemical study results, it
efficacy. Timing of additives, at what stage to add, is
was found that pot filled up to 3/4th capacity was most
also important. This is relevant to ingredients and the
suitable for fermenting Dasamularishta. Presence of total
environmental conditions under which the fermentation
phenolics, alkaloids, flavonoids and saponins in the
process is undertaken. Equally important is the method
marketed Dasamularishta and in the in-house preparation
for addition of additives; mixing, spreading or pottali in
was analysed on a UV spectrophotometer (Shimadzu
liquid ingredients should be deliberate. These different
1800 and Cyclomixer, Remi). Percent total phenolic
factors will impact the clinical efficacy. In case of
content was found to be more in the in-house preparation
process standardization: Ancient method avoid direct
than the marketed formulation, whereas the total
exposure to sunlight to maintain constant temperature;
flavonoid, alkaloid and saponin content was less in the
but other factor like humidity should also be studied.
in-house preparation than the marketed formulation.
Artificial maintenance of temperature and its effect on
Variations in geographical sources of raw materials and
the properties of the finished product is yet to be studied.
different methods adopted for their processing might
In case of finished product standardization: For different
have influenced these differences TLC showed two spots
formulations the period of maturation varies. There is a
under UV light with the solvent system n-butanol:glacial
need to evaluate the need for addition of preservative and
acetic acid:water (4:4:2) when sprayed with alcoholic
other effects, if any. The Central Council for Research in
KOH.
Ayurveda and Siddha (CCRAS) and Pharmacopoeia
laboratory for Indian medicine have notified standard
Kumariasava
protocol for quality control of asava-arishta. The
Alcohol content of Kumaryasava was determined using
compliance of pharmacopoeia standards for compound
both specific gravity as well as GC (Chemito GC7610
formulations does help in achieving uniformity and
Carbowax 20M) method. The result showed gradual
consistency in commercial production of Ayurvedic
reduction in ethanol content on storage of Kumaryasava
drugs. The limitations which arise for the standardization
in different containers, which may be due to vaporization
of classical dosage form can also be looked upon as a
on opening of the container. Therefore, asava and arista
scope for newer research for a better understanding of
preparations have to be consumed within a shorter period
the principles and processes, better end product with
of time or the formulation can be prepared in smaller
improved clinical efficacy. To bridge the gap between
volume. Total phenolic content was found to be 0.1 %.
traditional concepts and modern parameters it is
According to Dash et al the limit of total phenolic
desirable to find solutions with deeper understanding of
compound should not be less than 0.6 % w/v.
principles for the use of modern technologies