Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Punjab 38000, Pakistan.
Department of Pharmaceutics, Faculty of Pharmacy, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan.
Molecules. 2022 Jul 11;27(14):4433. doi: 10.3390/molecules27144433.
The current study reports the fabrication of co-combination gel using Pregabalin and Withania coagulans fruit extract to validate its effectiveness for neuropathic pain in chronic constriction injury (CCI) rat models. Three topical gels were prepared using Carbopol 934 through a pseudo-ternary phase diagram incorporating the Pregabalin (2.5%), Withania coagulans extract (2%), and co-combination of both Pregabalin (2.5%) and Withania coagulans extract (2%). Gels were characterized. FTIR showed a successful polymeric network of the gel without any interaction. The drug distribution at the molecular level was confirmed by XRD. The AFM images topographically indicated the rough surface of gels with a size range from 0.25 to 330 nm. DSC showed the disappearance of sharp peaks of the drug and extract, showing successful incorporation into the polymeric network of gels. The in vitro drug release of co-combination gel was 73% over 48 h. The mechanism of drug release by combination gel was Higuchi+ fickian with values of n (0.282) and R2 (0.947). An in vivo study for pain assessment via four methods: (i) heat hyperalgesia, (ii) cold allodynia, (iii) mechano-hyperalgesia, and (iv) dynamic mechano-allodynia, confirmed that topical treatment with co-combination gel reduced the pain significantly as indicated by the p value: R1 (p < 0.001), R2 (p < 0.001), R3 (p < 0.015), and R4 (p < 0.0344). The significance order was R2 () > R1 () > R3 (**) > R4 () > R5 (ns).
本研究报告了使用普瑞巴林和茄果提取物制备共组合凝胶,以验证其在慢性缩窄性损伤(CCI)大鼠模型中治疗神经病理性疼痛的有效性。通过伪三元相图制备了三种包含卡波姆 934 的局部用凝胶,其中加入了普瑞巴林(2.5%)、茄果提取物(2%)以及普瑞巴林(2.5%)和茄果提取物(2%)的共组合。对凝胶进行了特征描述。FTIR 显示凝胶的聚合物网络成功形成,没有任何相互作用。XRD 证实了药物在分子水平上的分布。AFM 图像从拓扑上表明凝胶具有 0.25 至 330nm 的粗糙表面。DSC 显示药物和提取物的尖锐峰消失,表明成功地将其掺入凝胶的聚合物网络中。共组合凝胶的体外药物释放 48 小时内达到 73%。组合凝胶的药物释放机制为 Higuchi+Fickian,n 值为 0.282,R2 值为 0.947。通过四种方法(i)热痛觉过敏、(ii)冷触诱发痛、(iii)机械性痛觉过敏和(iv)动态机械性触诱发痛,进行体内疼痛评估研究,证实局部使用共组合凝胶可显著减轻疼痛,p 值分别为:R1(p<0.001)、R2(p<0.001)、R3(p<0.015)和 R4(p<0.0344)。显著性顺序为 R2()>R1()>R3(**)>R4()>R5(ns)。