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Release of Chlorambucil from Poly( N ‐isopropylacrylamide) Hydrogels with β ‐Cyclodextrin Moieties
Author(s) -
Liu YuYang,
Fan XiaoDong,
Hu Hui,
Tang ZhongHua
Publication year - 2004
Publication title -
macromolecular bioscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.924
H-Index - 105
eISSN - 1616-5195
pISSN - 1616-5187
DOI - 10.1002/mabi.200400037
Subject(s) - self healing hydrogels , chemistry , poly(n isopropylacrylamide) , polymer , cyclodextrin , swelling , polymer chemistry , beta cyclodextrins , drug carrier , copolymer , chemical engineering , organic chemistry , drug delivery , engineering
Summary: The present work is focused on investigating the behavior of controlled drug release poly( N ‐isopropylacrylamide) (PNIPA) hydrogels in the presence of β ‐cyclodextrin ( β ‐CD). For this purpose, three types of NIPA hydrogels with β ‐CD moieties were synthesized with different architectures according to our previous studies. An anti‐cancer drug (chlorambucil, CLB), which can form an inclusion complex with β ‐CD, was selected for loading and in vitro release studies. The drug was loaded into hydrogels via a swelling method. DSC was used to study the interactions between the CLB molecules and the polymers. The results indicate that the CLB‐polymer interactions are at the molecular level. Loading CLB into these polymers can result in an evident decrease in the glass transition temperature ( T g ), and the variation of T g (Δ T g ) depends on the structures of the polymers and their β ‐CD content. The controlled release experiments show that the presence of β ‐CD can markedly enhance CLB release from shrunken PNIPA hydrogels and increase the ratio of CLB released in total drug loading content.Release profile of CLB from hydrogels 1a‐c and 4 at pH 1.4 and 7.4, at 37 °C.