Open AccessComputational pharmacokinetics and in vitro-in vivo correlation of anti-diabetic synergistic phyto-composite blend
Author(s) -
Baishakhi De,
Koushik Bhandari,
Nishant Chakravorty,
Ranjan Mukherjee,
Rohit Gundamaraju,
Rajeev K. Singla,
Prakash Katakam,
Shanta Kumari Adiki,
Biswajoy Ghosh,
Analava Mitra
Publication year - 2015
Publication title -
world journal of diabetes
Language(s) - English
Resource type - Journals
ISSN - 1948-9358
DOI - 10.4239/wjd.v6.i11.1179
Subject(s) - in silico , medicine , in vivo , pharmacology , pharmacokinetics , computational biology , drug development , bioinformatics , drug , microbiology and biotechnology , biology , biochemistry , gene
Despite tremendous strides in modern medicine stringent control over insulin resistance or restoration of normoglycemia has not yet been achieved. With the growth of molecular biology, omics technologies, docking studies, and in silico pharmacology, modulators of enzymes and receptors affecting the molecular pathogenesis of the disease are being considered as the latest targets for anti-diabetic therapy. Therapeutic molecular targets are now being developed basing on the up or down regulation of different signaling pathways affecting the disease. Phytosynergistic anti-diabetic therapy is in vogue both with classical and non-classical medicinal systems. However its chemo-profiling, structural and pharmacokinetic validation awaits providing recognition to such formulations for international acceptance. Translational health research with its focus on benchside product development and its sequential transition to patient bedside puts the pharma RDs to a challenge to develop bio-waiver protocols. Pharmacokinetic simulation models and establishment of in vitro-in vivo correlation can help to replace in vivo bioavailability studies and provide means of quality control for scale up and post approval modification. This review attempts to bring different shades highlighting phyto-synergy, molecular targeting of antidiabetic agents via different signaling pathways and bio-waiver studies under a single umbrella.