DSpace Repository

Chemoprofiling of Homoeopathic drug Holarrhena antidysenterica L.

Show simple item record

dc.contributor.author Mishra, Rakhi
dc.contributor.author Kumar, Manoj
dc.contributor.author Dwivedi, Binit
dc.contributor.author Arya, B.S.
dc.contributor.author Arya, Renu
dc.contributor.author Khurana, Anil
dc.contributor.author Manchanda, Raj K.
dc.date.accessioned 2019-04-11T07:14:33Z
dc.date.available 2019-04-11T07:14:33Z
dc.date.issued 2018
dc.identifier.citation Indian Journal of Research In Homoeopathy Vol.12 (4) en_US
dc.identifier.uri http://aohindia.in:8080/xmlui/handle/123456789/1857
dc.description.abstract Background: Chemoprofiling of homoeopathic drug/tincture (HT) represents a comprehensive approach for evaluation of quality, purity, safety and efficacy of HT. This paper reflects the chemoprofiling of Homoeopathic drug Holarrhena antidysentrica L. Objective: The objective of this study is to standardise Holarrhena antidysenterica mother tincture by taking the samples from four different sources: Dr D. P. Rastogi, CRI (H) Noida (A) and three from market (labelled as B, C and D). Materials and Methods: The authentic sample of bark of Holarrhena antidysenterica supplied by the Centre of Medicinal Plants Research in Homoeopathy, Emerald, Tamil Nadu, India was used to prepare the mother tincture (as per the Homoeopathic Pharmacopoeia of India). The solvents used throughout the study, namely, ethanol, high‑pressure liquid chromatography water, cyclohexane, chloromethane and diethylamine, were of analytical grade purity (MERCK Ltd.). Physicochemical properties, ultraviolet (UV) spectroscopy and high‑performance thin‑layer chromatography (HPTLC) chemoprofile of raw drug and mother tinctures were standardised and compared with market samples. Results: The present study reveals the moisture content (14.40%), total ash (4.65%), alcohol (18.0%), water extractive values (16.0%), total solids (1.47%), weight/ml (0.92 g) and alcohol content (60.6%). In UV spectroscopy, λmax values were observed at 228 and 278 nm in HT. HPTLC analysis of in‑house HT (A) and three market samples (B, C, D) was performed by using cyclohexane: chloromethane: diethylamine (7:3:1, v/v/v) as mobile phase. Under UV light (254, 366 nm) and in the presence of visualising agent Dragendroff, bands of active constituent were observed in all the four samples. However, excess amount of active constituents were found in in‑house HT (a) rather than the market samples (B, C and D). Conclusion: The present physicochemical and phytochemical data may be considered as pharmacopoeia standards for the homoeopathic drug Holarrhema antidysentrica L. en_US
dc.description.sponsorship CCRH en_US
dc.language.iso en en_US
dc.subject Drug standardisation en_US
dc.subject High‑performance thin‑layer chromatography en_US
dc.subject High‑performance thin‑layer chromatography fingerprint en_US
dc.subject Homoeopathic drug en_US
dc.subject Physicochemical en_US
dc.subject Ultraviolet en_US
dc.title Chemoprofiling of Homoeopathic drug Holarrhena antidysenterica L. en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account