Standardization and evaluation of herbal medicinal preparations
standardization & evaluation of herbal medicinal preparations 1BN PG Girls College of Pharmacy, Udaipur-
Raj.INDIA 313 002
: – In recent years there has been huge demand for plant-derived products in the developed countries. These products are increasingly used as medicines, food supplements & cosmetics sought. (1) There are about 6,000 vegetable producers in India. More than 4,000 units produced Ayurvedic medicine. Due into lack of infrastructure, skilled manpower, reliable methods & strict legal rules, most of these manufacturers produce their products at a very conservative basis. (2)
The standardization of crude drug materials include the following steps: –
authentication: – Each step must be authenticated.
a) phase of the collection.
Leaf constant: – palisade ratio, vein island number, vein termination stomatal number & stomatal index. Trichomes. Stomata. Quantitative Microscopy. Taxonomic identity. Foreign body. Sensory evaluation. Ash values & extractive values. Moisture content determination. Chrometographic & spectroscopic analysis. Heavy metal determination. Pesticide residues. Microbial contamination. Radioactive contamination.
herbal formula in general can be schematically standardize into the drug with raw materials from different places & a comparative chemical action must be formulated in different batches collected formulation observed. The preparations with better clinical efficacy are into be selected. be reviewed after all the routine physical, chemical & pharmacological parameters for all lots into select the final finished product & validate the entire manufacturing process. (6)
color, odor include, appearance, clarity, viscosity, moisture, pH, disintegration time, friability, hardness, flow properties, flocculation, sedimentation, settling velocity & ash values.
limit tests, chemical tests, chemical tests can etc.of herbs with TLC, HPLC, HPTLC, GC, UV, GC-MS, fluorimetry, etc.
total viable content, total mold count of enterobacteria & their total count. Limiter as a quantitative or semi-quantitative tool into identify & control the amount of impurities such as reagents during abstraction can be used by different herbs are used come directly from impurities in the manufacture of ships & the solvent etc.
The topic of the herbal drug standardization massively wide & deep. The WHO guidelines can be summarized as follows: –
: – Sensory evaluation, foreign body, microscopy measurement.
fluorescence quenching use of fingerprints & marker compounds for identification & standardization of botanical drugs are used Densitometric thin layer chromatographic determination of escin in a herbal medicine with Asculum & Vitis dry Determination of stigmasterol, beta – sitosterol & stigma stanine in oral dosage forms using HPLC with evaporative light scattering detection: – Elemental analysis of herbal preparations for traditional medicines by neutron activation analysis with the standardization method kO: – liquid chromatography & liquid chromatography-UV determination Atmospheric pressure chemical ionization mass spectrometric characterization of sitosterol & stigmasterol in soybean oil: – Simultaneous determination of cinnamaldehyde, eugenol & paeonol in traditional Chinese medicine preparations by capillary GC FID: – HPTLC fingerprinting of the marketed formulation with Shankhpushpi: biological parameters (bioassay ):- adaptogenic activity profile evaluation of the herbal preparation: – help Evaluation of the antioxidant activity of herbal products: – assessment of microbial contamination reduction on plants through technological process of decoction & spray dry: – The technological process of raw material has many phases, usually, unwanted microbial growth but the complete elimination is used by the training & working condition. The goal of this study was into evaluate the microbial contamination, such as mineral solution (SE) & check spray dried extract (PSA) with the purpose of evaluation of reduction of contamination after boiling & spray dry. The microbiological analysis of the products was carried out of a total of germs & bacteria MPN. (19)
Evaluation of nitric oxide scavenging activity of selected medicinal plants in inflammatory diseases : – Four traditional medicinal plants, namely Ventilago madraspatana Gaertn., Rubia cordifolia Linn., Lanatana Camara Linn. And Morinda citrifolia Linn Were. for a study on the inhibition of nitric oxide (NO), a central role in the phenomenon of inflammation indicates the presence of effective anti-inflammatory components selected in it. Plant samples were spiked with different solvents into evaluate their inhibitory effect on NO produced in vitro from sodium nitroprusside & extracted in LPS-activated murine peritoneal macrophages ex vivo (20).The lipid peroxidation inhibitory activity: – The reaction mixture contained mice liver homogenate (0.2 ml, 10% w / v) in 0.15 KCl, KCl (0.1 ml, 150 pm ), Tris buffer (0.4 ml, pH 7.5) & various concentrations of test extracts. In vitro lipid peroxidation initiated by the addition of FeSO4.7H2O (0.1 ml, 10 pm). The reaction mixture was incubated at 37o 1 h after the incubation period was the reaction by adding thiobarbituric acid (TBA-2 ml, 0.8% finished) & min by heating the contents for 15th for the development of colored complex. The tubes were then at 4000 rpm for centrifuged for 10 minutes. cool and. The% inhibition of lipid peroxidation was determined by comparing the results of the test substance with those of the control never treated with extracts by monitoring the intensity determined at 532 nm. gallic acid was used as positive control. (21) evaluation of the marketed antidiabetic polyherbal formulatios with biomarkers: – in vivo & Shoe in vitro evaluation of hair growth potential of flower: Clinical evaluation of the safety & efficacy of herbal medicine coded “Dysmo-off” vs traditional medicine “Diclofenac sodium “Check for the treatment of primary dysmenorrhea: – Thermographic Rating: Biochemical Rating: Evaluation Kutaj-Ghanavati for alkaloidal principles: – Sensory Evaluation:
The theme is the herbal drug standardization massively wide & deep. It is so much into know & so much seemingly contradictory theories about herbal medicine & its relationship with human physiology & mental functions.
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Apers S, Naessens T, Pieters L., Vlietinck A. “Densitometric thin-layer chromatographic determination of escin in a herbal medicinal product of Aesculus & Vitis dry”, Jr. of the chromatographic analysis, vol.1112 (1 – 2), April 2006, pp.165-170. VD Nair, I. Kanfer, Hoogmartens J., “Determination of stigmasterol, beta-sitosterol & stigma stanine in oral dosage forms using HPLC with evaporative light scattering detection”, Journal of pharmaceutical & biomedical Analysis, vol. 41 (3), June 2006, pp. 731-737. Sarmani SB, Abugassa I., Hamzah A., MD Yahya, “Elemental analysis of herbal preparations for traditional medicines by neutron activation analysis with the standardization method kO” , Biological Trace Element Research, 1999, pp. 365-376. Careri M., Elviri L., A. Mangia, Liquid chromatography-UV determination & liquid chromatography-atmospheric pressure chemical ionization mass spectrometric characterization of sitosterol & stigmasterol in soybean oil “, Jr. of the chromatographic analysis, vol. 935 (1-2), Nov.2001, pp.249-257. Yu BS, SG Lai, Tan QL, “Simultaneous determination of cinnamaldehyde, eugenol & paeonol by in traditional Chinese medicine preparations capillary GC-FID, chemical & pharmaceutical Bulletin, vol. 54 (1), Jan 2006, pp. 114-116. MK Santosh, Shaila D., Sanjeeva Rao, I., “Standardization & study of dadimastaka pushyannga Churnas” Asian Jr. of Chemistry, vol. 16 (34), 2004, pp. 1735-1741. 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