Abstract

Ketorolac tromethamine is a non-steroidal anti-inflammatory drug used in the management of severe pain. The half-life of Ketorolac tromethamine is within the range of 2.5–4 h. Hence, repeated doses of Ketorolac tromethamine are needed in a day to maintain the therapeutic level. However, taking several doses of Ketorolac tromethamine in a day generates certain complications, such as acute renal failure and gastrointestinal ulceration. Therefore, a polymeric-controlled drug delivery system is needed that could prolong the release of Ketorolac tromethamine. Therefore, in the current study, pH-responsive carbopol 934/sodium polystyrene sulfonate-co-poly(acrylic acid) (CP/SpScPAA) hydrogels were developed by the free radical polymerization technique for the controlled release of Ketorolac tromethamine. Monomer acrylic acid was crosslinked with the polymers carbopol 934 and sodium polystyrene sulfonate by the cross-linker N’,N’-methylene bisacrylamide. Various studies were conducted to evaluate and assess the various parameters of the fabricated hydrogels. The compatibility of the constituents used in the preparation of hydrogels was confirmed by FTIR analysis, whereas the thermal stability of the unreacted polymers and developed hydrogels was analyzed by TGA and DSC, respectively. A smooth and porous surface was indicated by SEM. The crystallinity of carbopol 934, sodium polystyrene sulfonate, and the prepared hydrogels was evaluated by PXRD, which revealed a reduction in the crystallinity of reactants for the developed hydrogels. The pH sensitivity of the polymeric hydrogel networks was confirmed by dynamic swelling and in vitro release studies with two different pH media i.e., pH 1.2 and 7.4, respectively. Maximum swelling was exhibited at pH 7.4 compared to pH 1.2 and, likewise, a greater percent drug release was perceived at pH 7.4. Conclusively, we can demonstrate that the developed pH-sensitive hydrogel network could be employed as a suitable carrier for the controlled delivery of Ketorolac tromethamine.

Highlights

  • An ideal controlled drug delivery system (CDDS) is one that delivers the drug locally or systemically at a predetermined rate for a specified period of time

  • This all shows the development of Carbopol 934 (CP)/SpScPAA hydrogels due to the grafting of Acrylic acid (AA) on the backbone of CP and sodium polystyrene sulfonate (SpS)

  • A minor change is seen in the distinct peaks of the drug in the Fourier Transform Infrared (FTIR) spectrum of drug-loaded CP/SpScPAA hydrogels (Figure 1F)

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Summary

Introduction

An ideal controlled drug delivery system (CDDS) is one that delivers the drug locally or systemically at a predetermined rate for a specified period of time. The main goals of CDDSs are to ensure safety and enhance drug efficacy with improved patient compliance [1]. They are involved in the delivery of drugs to a specific/target site in the body. Due to the chemical or physical cross linking, these systems are not dissolved by the respective medium [6,7]. Both physical and chemical crosslinking methods are used in the development of hydrogel formulations [8,9]

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