Injectable thermosensitive gelling delivery system for the sustained release of lidocaine

被引:21
作者
Svirskis, Darren [1 ]
Chandramouli, Kaushik [1 ]
Bhusal, Prabhat [1 ]
Wu, Zimei [1 ]
Alphonso, Jolyene [1 ]
Chow, Joyce [1 ]
Patel, Divya [1 ]
Ramakrishna, Riddhi [1 ]
Yeo, Seung J. [1 ]
Stowers, Renus [2 ]
Hill, Andrew [2 ]
Munro, Jacob [3 ]
Young, Simon W. [3 ]
Sharma, Manisha [1 ]
机构
[1] Univ Auckland, Sch Pharm, Fac Med & Hlth Sci, Private Bag 92019, Auckland 1142, New Zealand
[2] Univ Auckland, Dept Surg, Middlemore Hosp, Fac Med & Hlth Sci, South Auckland Clin Campus, Auckland, New Zealand
[3] Univ Auckland, Sch Med, Fac Med & Hlth Sci, Auckland, New Zealand
关键词
arthroplasty; in situ gelling system; poloxamers; sol-gel transition; surgery; sustained release; thermoreversible; thermosensitive; total joint replacement;
D O I
10.4155/tde-2016-0014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Patients undergoing arthroplasty require appropriate postsurgical pain relief. Analgesia is typically achieved through bolus doses of short-acting local anesthetics and with oral analgesics such as opiates, which are associated with systemic side effects. By formulating an injectable thermosensitive gelling system containing lidocaine, sustained and local delivery can be achieved following a single administration. Results: Poloxamer-based thermosensitive gelling formulations were prepared. Altering the weight ratios of poloxamers affected the sol-to-gel transition temperature, mechanical and rheological properties and in vitro drug release. Desirable formulations gelled between 28 and 33 degrees C providing sustained release of lidocaine over 48 h. Conclusion: Thermosensitive gelling systems are promising for sustained drug release following patient administration and may be beneficial in addressing postoperative pain.
引用
收藏
页码:359 / 368
页数:10
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