نتایج جستجو برای: olanzapine 2 hydroxypropyl β cyclodextrin inclusion complex

تعداد نتایج: 3365393  

2015
Mohammad Ansari

Article history: Received on: 26/07/2015 Revised on: 15/08/2015 Accepted on: 09/09/2015 Available online: 27/09/2015 Objective To evaluate the effect of Polyethylene glycol and β-cyclodextrin on the solubility and dissolution of silymarin, a poorly water soluble herbal drug. Methodology Effects of beta cyclodextrins and Polyethylene glycol on solubility of silymarin were evaluated by phase solu...

2013
Shaimaa M. Badr-Eldin Tarek A. Ahmed Hatem R Ismail

OBJECTIVE(S) The aim of this work was to investigate the effect of the natural and the chemically modified form of cyclodextrins namely; β-cyclodextrin (β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD) respectively on the solubility and dissolution rate of aripiprazole; an antipsychotic medication showing poor aqueous solubility. MATERIALS AND METHODS Phase solubility of aripiprazole with the...

A Yakoob Khan F Jalees Ahmad R Kishan Khar S Talegaonkar Z Khan

Paracetamol is a sparingly soluble bitter tasting drug. It is widely used as an analgesic and antipyretic. Complexation of drug with different cyclodextrins (?, ? and HP-?-CD) was attempted to improve solubility of Paracetamol. During the drug excipient interaction studies, ?, ? cyclodextrins elicited analytical interference and showed considerable absorbance at ?max (243.5 nm) of Paracetamol w...

Journal: :Applied Biochemistry and Biotechnology 2021

In the present work, we tried to identify mechanism why by which steroid alcohols accumulated when hydroxypropyl-β-cyclodextrin (HP-β-CD) was enhance sterol conversion rate. Compared with bioconversion system without HP-β-CD, reaction rate greatly improved in presence of but largely concurrently. a an enhanced rate, higher intracellular NADH/NAD+ level detected, and production increased also. M...

2013
Payal H. Patil Veena S. Belgamwar Pratibha R. Patil Sanjay J. Surana

The objective of the present work was to enhance the solubility and dissolution of practically water-insoluble drug raloxifene HCl (RLX), for the same two approaches that were used. In the first approach, drug was kneaded with hydroxypropyl-β-cyclodextrin (HPβCD), and in the second one drug was cogrinded with modified guar gum (MGG). The drug-cyclodextrin complex and drug-MGG cogrind mixtures w...

2017
Vaishali Tejas Thakkar Amol Deshmukh Lal Hingorani Payal Juneja Lalji Baldaniya Asha Patel Tosha Pandya Mukesh Gohel

INTRODUCTION The Bacopa monnieri is traditional Ayurvedic medicine, and reported for memory-enhancing effects. The Bacoside is poorly soluble, bitter in taste and responsible for the memory enhancement action. Memory enhancer is commonly prescribed for children or elder people. OBJECTIVE Poor solubility, patient compliance and bitterness were a major driving force to develop taste masked β-cy...

2017
Krishna Pillai Javed Akhter David Lawson Morris

Poor aqueous solubility of anticancer drug, albendazole (ABZ), prevents parenteral application. Here, we demonstrate how to increase the aqueous solubility of ABZ to 6- 8 mg/ml using sulfobutylether - β-cyclodextrin (SBE-β-CD) or Hydroxypropyl- β-cyclodextrin (HP- β-CD) by manipulation of complexation parameters such as the physical state of ABZ (ionized in acetic acid), the concentration of io...

Journal: :Dalton transactions 2012
Koji Kano Syoichi Chimoto Mariko Tamaki Yoshiki Itoh Hiroaki Kitagishi

Three types of per-O-methylated β-cyclodextrin dimers, Im2CD, Im3NHCD and Py3NHCD, were prepared as globin models. Im2CD was synthesized by the condensation reaction of mono(2(A)-amino)-per-O-methylated β-cyclodextrin with 3-(1H-imidazol-1-yl)pentanedioic acid. Im3NHCD and Py3NHCD were obtained through the S(N)2 reactions of mono(2(A),3(A)-epoxy)-per-O-methylated β-cyclodextrin with 3-(1H-imida...

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