Preparation, in vitro and in vivo evaluation of solid-state self-nanoemulsifying drug delivery system (SNEDDS) of vitamin A acetate محمد خالد انور
Proniosomal transdermal therapeutic system of losartan potassium: development and pharmacokinetic evaluation. محمد خالد انور
Spectroscopic characterization of fulvic acids extracted from the rock exudate Shilajit محمد خالد انور
Organic Geochemistry 39 (2008) 1719–1724. (impact factor - 2.828).
Rajesh Khanna , Matthias Witt , Md. Khalid Anwer, Suraj P. Agarwal, Boris P. Koch.
Complexation of furosemide with fulvic acid extracted from shilajit: a novel approach. محمد خالد انور
Physico-chemical, Spectral and Thermal Characterization of Shilajit, A Humic Substance with Medicinal Properties. محمد خالد انور
Asian J. Chem. 2008, 20(1): 209-217.
SURAJ P. AGARWAL, RAJESH KHANNA‡, RITESH KARMARKAR, MD. KHALID ANWER and ROOP K. KHAR.
Enhancement of the Dissolution and Diuretic Effect of Furosemide Through a Novel Complexation with Humic Acid Extracted from Shilajit. محمد خالد انور
Asian J. Chem. 2007, 19(6): 4711-4718.
SURAJ P. AGARWAL, MOHD. AQIL and MD. KHALID ANWER
Shilajit: a review محمد خالد انور
Development and validation of Reverse phase HPLC method and enhancement of water solubility and bioactivity of diosmin and/or hesperidin Using cyclodextrin محمد خالد انور
The aim of proposed project is to develop reversed-phase HPLC methods for the determination of diosmin and hesperidin simultaneously and/or or separately. The methods will be applied for determination of the diosmin and/or hesperidin in plant extract and pharmaceutical dosage forms. Diosmin and hesperidin are natural substances with a lot of biological activities, including the antioxidant one. Their use in pharmaceutical field is, however, limited by their aqueous insolubility. As the formation of the inclusion complexes can improve their solubility in water, the diosmin and/or hesperidin will be complexed with cyclodextrin by the kneading method and the complexes will be evaluated for drug inclusion, solubility, DSC, FT-IR spectroscopy and dissolution study. In vitro dissolution profiles of the formulations from the optimized complexes will be compared with those of the non-complexed and marketed formulations in simulated gastric and intestinal fluid to mimic the bioavailability.
Discovery and computer-aided drug design studies of the anticancer marine triterpene sipholanes as novel P-gp and Brk modulators. In: Anticancer drugs from marine origin أحمد ابراهيم فودة
Foudah, A. I.; Sallam, A. A.; El Sayed, K. A., Discovery and computer-aided drug design studies of the anticancer marine triterpene sipholanes as novel P-gp and Brk modulators. In: Anticancer drugs from marine origin, eds, Se-Kwon Kim, Springer Publishers
In silico and in vitro screening of natural products library: Identification of FAK inhibitor targeting Y397 site in breast cancer أحمد ابراهيم فودة
Akl, M. R.; Foudah, A. I.; Ebrahim, H. Y.; El Sayed, K. A. In silico and in vitro screening of natural products library: Identification of FAK inhibitor targeting Y397 site in breast cancer. J. Nat. Prod. 2014