Injectable thermosensitive gelling delivery system for the sustained release of lidocaine

Author:

Svirskis Darren1,Chandramouli Kaushik1,Bhusal Prabhat1,Wu Zimei1,Alphonso Jolyene1,Chow Joyce1,Patel Divya1,Ramakrishna Riddhi1,Yeo Seung J1,Stowers Renus2,Hill Andrew2,Munro Jacob3,Young Simon W3,Sharma Manisha1

Affiliation:

1. School of Pharmacy, Faculty of Medical & Health Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand

2. Department of Surgery, South Auckland Clinical Campus, Middlemore Hospital, Faculty of Medicine & Health Sciences, University of Auckland, New Zealand

3. School of Medicine, Faculty of Medical & Health Sciences, University of Auckland, New Zealand

Abstract

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°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.

Publisher

Future Science Ltd

Subject

Pharmaceutical Science

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