several plant extracts and phytoconstituents, despite having excellent bioactivity in vitro, demonstrate less or no in vivo actions due to their poor lipid solubility or improper molecular size or destruction in gut. drug delivery system for polyphenolic phytoconstituents (phytosomes) was prepared by complexing polyphenolic phytoconstituents with phospholipid mainly phosphatidylcholine which bi...

Identification of the usefulness of lipid-based formulations (LBFs) for delivery of poorly water-soluble drugs is at date mainly experimentally based. In this work we used a diverse drug data set, and more than 2,000 solubility measurements to develop experimental and computational tools to predict the loading capacity of LBFs. Computational models were developed to enable in silico prediction ...

Polysorbates and Pluronic polymers are straightforward to use improve the performance of hydrophobic molecules, however, colloidal systems these not fully understood loading drug molecules in Polysorbate micelles rely on a plethora factors. Thus, it is laborious task select optimal as delivery vehicle. To pave way for Polysorbates, three with different hydrophobicity were selected oral Olanzapi...

background: drug delivery systems related to different cancer therapy is now expanding. chitosan (cs) is currently receiving enormous interest for medical and pharmaceutical applications due to its biocompatibility in animal tissues. in this study two nanogels were prepared from chitosan. some of the critical factors such as controlling the release, adsorption and specially targeting drug deliv...

Human and animal leukemias, varying widely in responsive ness to 6-mercaptopurine, were examined to seek determinants of drug sensitivity. Drug-responsive rodent leukemias showed a comparatively high capacity for in vitro conversion of 6-mer captopurine into nondiffusible cellular metabolites, predomi nantly drug nucleotides. A similar study of human leukemia cells indicated that the in vitro c...

In this paper, the synthesis and free-radical scavenging capacity of novel calix[4]arene-based cluster of paracetamol was reported. The phenolic structures of acetaminophen and calix[4]arene prompted us for designing a synthetic route for calix[4]arene-based cyclic tetramer of paracetamol. The present chalice-shaped cluster is the first example of calixarene/acetaminophen hybrid and paracetamol...

In this paper, the synthesis and free-radical scavenging capacity of novel calix[4]arene-based cluster of paracetamol was reported. The phenolic structures of acetaminophen and calix[4]arene prompted us for designing a synthetic route for calix[4]arene-based cyclic tetramer of paracetamol. The present chalice-shaped cluster is the first example of calixarene/acetaminophen hybrid and paracetamol...

      Several plant extracts and phytoconstituents, despite having excellent bioactivity in vitro, demonstrate less or no in vivo actions due to their poor lipid solubility or improper molecular size or destruction in gut. Drug delivery system for polyphenolic phytoconstituents (phytosomes) was prepared by complexing polyphenolic phytoconstituents with phospholipid mainly phosphatidylcholine wh...

Some theories suggest that spontaneously activated, drug-related associations in memory may have a "freer reign" in predicting drug use among individuals with lower working memory capacity. This study evaluated this hypothesis among 145 at-risk youth attending continuation high schools (CHS). This is the 1st study to evaluate this type of dual-process interaction in the prediction of drug use a...