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DOI 10.1016/j.msec.2016.04.056

Медицинская библиотека · Materials science & engineering. C, Materials for biological applications · 2016

A new synthetic methodology for the preparation of biocompatible and organo-soluble barbituric- and thiobarbituric acid based chitosan derivatives for biomedical applications.

Shahzad Sohail, Shahzadi Lubna, Mahmood Nasir, Siddiqi Saadat Anwar, Rauf Abdul, Manzoor Faisal, Chaudhry Aqif Anwar, Rehman Ihtesham Ur, Yar Muhammad

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Аннотация

Chitosan's poor solubility especially in organic solvents limits its use with other organo-soluble polymers; however such combinations are highly required to tailor their properties for specific biomedical applications. This paper describes the development of a new synthetic methodology for the synthesis of organo-soluble chitosan derivatives. These derivatives were synthesized from chitosan (CS), triethyl orthoformate and barbituric or thiobarbituric acid in the presence of 2-butannol. The chemical interactions and new functional motifs in the synthesized CS derivatives were evaluated by FTIR, DSC/TGA, UV/VIS, XRD and (1)H NMR spectroscopy. A cytotoxicity investigation for these materials was performed by cell culture method using VERO cell line and all the synthesized derivatives were found to be non-toxic. The solubility analysis showed that these derivatives were readily soluble in organic solvents including DMSO and DMF. Their potential to use with organo-soluble commercially available polymers was exploited by electrospinning; the synthesized derivatives in combination with polycaprolactone delivered nanofibrous membranes.

Для цитирования: Shahzad Sohail, Shahzadi Lubna, Mahmood Nasir, Siddiqi Saadat Anwar, Rauf Abdul, Manzoor Faisal, Chaudhry Aqif Anwar, Rehman Ihtesham Ur, Yar Muhammad. A new synthetic methodology for the preparation of biocompatible and organo-soluble barbituric- and thiobarbituric acid based chitosan derivatives for biomedical applications.. Materials science & engineering. C, Materials for biological applications. 2016. DOI: 10.1016/j.msec.2016.04.056.

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