4.7 Article

Superiority of microemulsion-based hydrogel for non-steroidal anti-inflammatory drug transdermal delivery: a comparative safety and anti-nociceptive efficacy study

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DOI: 10.1016/j.ijpharm.2022.121830

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Cubosomal gel; Diclofenac; Irritation; Lipid-based nanocarriers; Microemulsion-based hydrogel; Proliposomal gel

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Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to manage pain caused by inflammatory disorders, but their oral administration often leads to side effects. This study explored the delivery of NSAIDs via the skin as an attractive alternative. Different types of gels, including microemulsion-based hydrogel (MBH), were prepared and loaded with diclofenac. The physicochemical properties, permeation ability, irritation effect, and antinociceptive efficacy of the gels were evaluated. MBH showed the highest permeation ability, as well as the best results in terms of irritation and toxicity. It was concluded that limonene-containing microemulsion hydrogel is a promising lipid-based vehicle for safe and effective pain treatment.
Non-steroidal anti-inflammatory drugs (NSAIDs) represent the foundation of pain management caused by inflammatory disorders. Nevertheless, their oral administration induces several side effects exemplified by gastric ulceration, thus, delivering NSAIDs via skin has become an attractive alternative. Herein, microemulsion-based hydrogel (MBH), proliposomal, and cubosomal gels were fabricated, loaded with diclofenac, and physicochemically characterized. The size, charge, surface morphology, and the state of diclofenac within the reconstituted gels were also addressed. The ex-vivo permeation study using Franz cells was performed via the rat abdominal skin. The formulations were assessed in-vivo on mice skin for their irritation effect and their antinociceptive efficacy through tail-flick test. Biosafety study of the optimal gel was also pointed out. The gels and their dispersion forms displayed accepted physicochemical properties. Diclofenac was released in a prolonged manner from the prepared gels. MBH revealed a significantly higher skin permeation and the foremost results regarding in-vivo assessment where no skin irritation or altered histopathological features were observed. MBH further induced a significant anti-nociceptive effect during the tail-flick test with a lower tendency to evoke systemic toxicity. Therefore, limonene-containing microemulsion hydrogel is a promising lipid-based vehicle to treat pain with superior safety and therapeutic efficacy.

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