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1.
J Mater Sci Mater Med ; 24(8): 1939-49, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23665921

ABSTRACT

A new strategy for the synthesis of thiolated carboxymethyl chitosan-g-cyclodextrin nanoparticles by an ionic-gelation method is presented. The synthetic approach was based on the utilization of 1,6-hexamethylene diisocyanate during cyclodextrin grafting onto carboxymethyl chitosan. The use of the 1,6-hexamethylene diisocyanate resulted in reactions between cyclodextrin and active sites at the C6-position of chitosan, and preserved amino groups of chitosan for subsequent reactions with thioglycolic acid, as the thiolating agent, and tripolyphosphate, as the gelling counterion. Various methods such as scanning electron microscopy, rheology and in vitro release studies were employed to exhibit significant features of the nanoparticles for mucosal albendazole delivery applications. It was found that the thiolated carboxymethyl chitosan-g-cyclodextrin nanoparticles prepared using an aqueous solution containing 1 wt% of tripolyphosphate and having 115.65 (µmol/g polymer) of grafted thiol groups show both the highest mucoadhesive properties and the highest albendazole entrapment efficiency. The latter was confirmed theoretically by calculating the enthalpy of mixing of albendazole in the above thiolated chitosan polymer.


Subject(s)
Albendazole/administration & dosage , Anthelmintics/administration & dosage , Chitosan/analogs & derivatives , Cyclodextrins/chemistry , Nanoparticles/chemistry , Pharmaceutical Vehicles/chemistry , Sulfhydryl Compounds/chemical synthesis , Albendazole/pharmacokinetics , Anthelmintics/pharmacokinetics , Body Fluids/metabolism , Chitosan/chemistry , Coated Materials, Biocompatible/chemical synthesis , Coated Materials, Biocompatible/chemistry , Cyclodextrins/chemical synthesis , Drug Compounding/methods , Humans , Intestinal Secretions/metabolism , Materials Testing , Pharmaceutical Vehicles/chemical synthesis , Sulfhydryl Compounds/chemistry
2.
Anal Sci ; 27(10): 1037-41, 2011.
Article in English | MEDLINE | ID: mdl-21985929

ABSTRACT

In this work, a combined discrete and continuous wavelet transform analysis was developed for simultaneous spectrophotometric determinations of metformin hydrochloride and glibenclamide, two antidiabetic drugs, in binary mixtures without any chemical pretreatment. Absorption spectra were subjected to the 4-level db4 discrete wavelet transform (DWT) for signal de-noising. Selected continuous wavelet transform (CWT) families (rbio3.1 with scaling factor, a = 80, and gaus2, a = 60) were applied on these de-noised signals. Finally, a zero-crossing technique was used for the construction of calibration curves for both drugs. The proposed method was validated by analyzing synthetic mixtures of the investigated drugs with various concentrations. The amount of metformin hydrochloride and glibenclamide were determined by using CWT amplitudes in zero-crossing points. The mean recovery values of metformin hydrochloride and glibenclamide were found between 98.6-102.0 and 97.9-102.4% for rbio3 and 98.3-101.2 and 97.1-101.4% for gaus2 families, respectively. The obtained results showed that the developed method is a simple, rapid and precise procedure for the simultaneous determination of metformin hydrochloride and glibenclamide in binary mixtures.


Subject(s)
Glyburide/analysis , Metformin/analysis , Wavelet Analysis , Complex Mixtures/chemistry , Spectrophotometry, Ultraviolet
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