Objective: To evaluate the pharmacognostical and phytochemical parameters of Physalis minima leaf. Methods: The leaf of Physalis minima was examined for macroscopical, microscopical, physicochemical parameters and fluorescence analysis. Extracts obtained from the leaf was analyzed for phytochemical screening and estimation of total tannin, phenolic and flavonoid content following the standard procedure available in the literature. Results: Morphologically, the leaf was found to be ovate in shape, 5 to 8 cm long and up to 3 cm width with dentate margin, asymmetrical base, hairy surface, reticulate veins on each side of midrib, green in colour, characteristic odour and slight bitter in taste. Microscopic study has shown the important diagnostic characters of Solanaceae family which is characterized by presence of dorsiventral leaf with anomocytic stomata, grandular or uniseriate trichomes and cluster crystal of calcium oxalate. Physicochemical parameters like foreign organic matter (0.78%), loss on drying (8.23%), total ash (11.4%), acid insoluble ash (2.2%), water-soluble ash (6.1%), sulphated ash (2.4%) alcohol soluble extractive (10.4%), water-soluble extractive (9.5%), ether soluble extractive (1.8%) foaming index (below 100), swelling index (1), volatile oil and heavy metal content were quantified. Phytochemical analysis of different extracts of Physalis minima leaf has shown the presence of phytoconstituents viz. alkaloids, steroids, tannin, flavonoids, protein. Quantification of phytoconstituents was also reported like phenols (10.59±0.65 mg/gm equivalent to tannic acid), tannin (8.24±0.27 mg/gm equivalent to tannic acid) and flavonoids (87.17±0.87 mg/gm equivalent to rutin) respectively. Conclusion: This present study was provided the qualitative and quantitative standard of Physalis minima will help to prevent the possible steps of adulteration with other species of the same genus.
Starch is one important natural polymer that finds application in the formulation of dosage forms as the binder, disintegrates, diluents, gelling agent etc. Starch is drawing the attention in drug delivery as it is cheap, non-toxic, renewable, biodegradable and compatible with many other materials for industrial application. Starch has vital intrinsic properties that have made its pharmaceutical applications possible. It has also been used for a wide range of particular drug delivery applications, such as the delivery of challenging molecules and targeting to specific sites in the body. Starches are integrally unsuitable for most applications such as loss of viscosity and thickening power upon cooking and storage, retrogradation characteristics and absence of certain groups responsible for a particular function etc. So, in order to reduce its limitations and improve its applications, modification of starch is necessary. It can be modified by several ways like chemical modification, physical modification and genetic modification but the most important one is the chemical modification. This review summarizes the properties and application of native starchin conventional drug delivery systems within a world of dynamic drug production technology. It also describes the chemical modification like cross-linking, esterification, etherification and dual modification of starch.
The aim of the study is to isolate and characterization of bioconstituent present in methanolic extract of Mirabilis jalapa L. tuber and also evaluate the cardioprotective property of the extract as well as isolated compound from the extract. The bioactive constituent flavonoid was isolated from methanolic extract through flash chromatography technique by using solvent system ethyl acetate and methanol. The chemical structure of compound was confirmed on the basis of spectroscopy analysis and identified as 2-(3′, 4′-dihydroxy phenyl)-3,5,7trihydroxy chromen 4-one. Administration of Mirabilis jalapa extract in higher dose 200 and 400 mg/kg b.w. and isolated compound to doxorubicin-intoxicated rats demonstrated prominent reduction in serum biomarker enzymes, normalization of serum lipid profiles. Also, significant modulation of malondialdehyde (MDA), endogenous non-enzymatic (GSH) and enzymatic (SOD and CAT) antioxidant and detoxification systems compared to doxorubicin control rats. This was achieved due to presence of flavonoid in the methanolic extract of Mirabilis jalapa L. tuber.
Inflammation is a vital therapeutic target for creating new methods for pharmacological interventions, aside from being a stage in the pathophysiology of many diseases, such as atherosclerosis and rheumatoid arthritis. Thus, molecular understanding of inflammation has led to new opportunities for drug creation and significant new implications for current clinical medicine. It has also revealed the biological targets and mechanisms of therapeutic action, opening up new opportunities to alter complex biological systems. Meanwhile, using medicinal plants to control inflammation has been recommended as an alternative to traditional therapeutic approaches for a variety of conditions, particularly when suppression of inflammation is anticipated. Several medicinal plant species have been demonstrated to have strong anti-inflammatory properties in contemporary research. The review article was discussed about the chemical constituents and biological properties of therapeutically active plants including curcumin from Curcuma longa and epigallocatechin-3-gallate from Camellia sinensis, including the molecular pharmacology of active constituents against inflammation.
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