Boswellia serrata Derived Phytochemicals against Dysentery

Dysentery is an intestinal inflammation, primarily of the colon. Nature is a major source of medicines for different diseases like Dysentery. Phytochemicals from Boswellia serrata plant extract can cure Dysentery. This objective of the study is to identify the phytochemical of Boswellia serrata capable of curing Dysentery. Molecular docking method applied using “Biovia DiscoveryStudio”. “High positive values of -CDOCKER energy and -CDOCKER interaction energy” suggested that p-cymene can effectively deactivate the enzyme, thereby interrupting the life cycle of the organism

Alpinia galanga Derived Phytochemicals against Shikimate Dehydrogenase Causing Peptic Ulcer

Phytochemicals can be derived from different parts of plants. Different medicinal plants and their phytoextracts have shown anti-microbial action. These medicinal plants play a key role in human health care. Phytochemicals from Alpinia galanga plant extract are traditionally used to cure PepticUlcer. The objective of the study is to identify the phytochemical of Alpinia galanga capable of curing Peptic Ulcer. Molecular docking method applied using “Biovia Discovery Studio”. “High positive values of -CDOCKER energy and -CDOCKER interaction energy” suggested that Alpinia galanga derived Phytochemicals cannot act effectively against Peptic Ulcer caused by Helicobacter pylori.

Syzygium aromaticum Derived Phytochemicals against Infections in Feet Crack Caused by Trichophyton rubrum

Phytochemicals from Syzygium aromaticum plant extract traditionally used to cure Feet Crack. Molecular docking method applied using “Biovia Discovery Studio”. “High positive values of -CDOCKER energy and -CDOCKER interaction energy” suggested that Myricetin can effectively deactivate the dihydrofolate reductase enzyme thereby interrupting the life cycle of the organism

Santalum album L. Derived Phytochemicals against Jaundice

Phytochemicals are produced by plants as secondary metabolites to protect the plants from predators. When the parts of the plant, which are rich in different phytochemical constituents, are consumed by humans, they can cure different diseases. Phytochemicals from Santalum albumplant extract are traditionally used to cure Jaundice. Molecular docking method applied using “Biovia Discovery Studio”. “High positive values of -CDOCKER energy and -CDOCKER interaction energy” suggested that Isohamnetin can effectively deactivate the enzyme, thereby interrupting the life cycle of the organism

Piper nigrum Derived Phytochemicals against Gonorrhoea

Phytochemicals from Piper nigrum plant extract are traditionally used to cure Gonorrhoea. It is caused by Neisseria gonnorrhoeae. Molecular docking method applied using “Biovia Discovery Studio”. “High positive values of -CDOCKER energy and -CDOCKER interaction energy” suggested that p-cymenecan effectively deactivate the dihydrofolate reductase enzyme thereby interrupting the life cycle of the organism

Formulation Design And Optimization Of Floating Matrix Tablets Of Ciprofloxacin Hcl By Using Hpmc And Ethyl Cellulose With Experimental Design

The oral floating matrix tablets of Ciprofloxacin Hydrochloride were formulated by Experimental design by using HPMC K100M and Ethyl Cellulose as the retardant polymers each with three different levels with an approach to increase gastric residence and thereby improve drug bioavailability. From FTIR results it was confirmed that there is no chemical interaction between the drug with the excipients used in tablet formulations. Also, there was no shift in the endotherm of in the drug- excipients mixtures indicating compatibility of drug with all the excipients. All the tablets were prepared by effervescent approach in which Sodium bicarbonate was added as a gas generating agent. Floating Matrix tablets were prepared by direct compression method and prepared tablets were evaluated for weight variation, percentage friability, hardness and drug content studies. All the formulations showed compliance with pharmacopeia standards (I.P. 1996). Floating lag times of all the formulations were within 1 minute and Total floating time of all the formulations were more than 12 hours. In vitro release studies revealed that the release rate decreased with increase polymer proportion of retarding polymers. The formulation CHE9 sustained release of drug for 12 hours with 21% release of drug after 1 hour and more than 97% at the end of 12 hours. From the Kinetic model it was found that the optimized formulation CHE9 showed linearity in case of Zero order (R2: 0.938) and Higuchi model (R2: 0.954). By fitting data to Korsmeyer-Peppas model and ‘n’ value lying above 0.5 indicating non Fickian release.