Thermosensitive Poloxamer 407/Poly(Acrylic Acid) Hydrogels with Potential Application as Injectable Drug Delivery System

被引:50
|
作者
Boonlai, Wannisa [1 ]
Tantishaiyakul, Vimon [2 ,3 ]
Hirun, Namon [1 ,4 ]
Sangfai, Tanatchaporn [1 ]
Suknuntha, Krit [2 ,3 ]
机构
[1] Walailak Univ, Sch Pharm, Nakhon Si Thammarat 80161, Thailand
[2] Prince Songkla Univ, Fac Pharmaceut Sci, Ctr Excellence Drug Delivery Syst, Hat Yai 90112, Thailand
[3] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmaceut Chem, Hat Yai 90112, Thailand
[4] Walailak Univ, Drug & Cosmet Excellence Ctr, Nakhon Si Thammarat 80161, Thailand
来源
AAPS PHARMSCITECH | 2018年 / 19卷 / 05期
关键词
poloxamer; 407; poly(acrylic acid); thermosensitive hydrogel; gelation temperature; PEO BLOCK-COPOLYMER; IN-SITU; AQUEOUS-SOLUTION; TRIBLOCK COPOLYMER; RHEOLOGICAL PROPERTIES; MECHANICAL-PROPERTIES; STRUCTURAL-PROPERTIES; POLY(ACRYLIC ACID); SUSTAINED-RELEASE; GEL;
D O I
10.1208/s12249-018-1010-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Thermosensitive hydrogels are of great interest for in situ gelling drug delivery. The thermosensitive vehicle with a gelation temperature in a range of 30-36A degrees C would be convenient to be injected as liquid and transform into gel after injection. To prepare novel hydrogels gelling near body temperature, the gelation temperature of poloxamer 407 (PX) were tailored by mixing PX with poly(acrylic acid) (PAA). The gelation behaviors of PX/PAA systems as well as the interaction mechanism were investigated by tube inversion, viscoelastic, shear viscosity, DSC, SEM, and FTIR studies. The gelation temperature of the plain PX solutions at high concentration of 18, 20, and 22% (w/w) gelled at temperature below 28A degrees C, which is out of the suitable temperature range. Mixing PX with PAA to obtain 18 and 20% (w/w) PX with 1% (w/w) PAA increased the gelation temperature to the desired temperature range of 30-36A degrees C. The intermolecular entanglements and hydrogen bonds between PX and PAA may be responsible for the modulation of the gelation features of PX. The mixtures behaved low viscosity liquid at room temperature with shear thinning behavior enabling their injectability and rapidly gelled at body temperature. The gel strength increased, while the pore size decreased with increasing PX concentration. Metronidazole, an antibiotic used for periodontitis, was incorporated into the matrices, and the drug did not hinder their gelling ability. The gels showed the sustained drug release characteristic. The thermosensitive PX/PAA hydrogel could be a promising injectable in situ gelling system for periodontal drug delivery.
引用
收藏
页码:2103 / 2117
页数:15
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