Department of Pharmaceutics, Institute of Pharmacy, Nirma University, SG Highway, Ahmedabad 382481, India.
Department of Pharmaceutics, Institute of Pharmacy, Nirma University, SG Highway, Ahmedabad 382481, India.
Int J Pharm. 2023 Jul 25;642:123144. doi: 10.1016/j.ijpharm.2023.123144. Epub 2023 Jun 16.
Oral cancer accounts for more than 350,000 cases worldwide with 90% of them being oral squamous cell carcinomas (OSCC). The current treatment modalities of chemoradiation have poor outcomes along with harmful effects to neighbouring healthy tissues. The present study aimed to deliver Erlotinib (ERB), locally at the site of tumor arising in the oral cavity. ERB was encapsulated in liposomal formulations (ERB Lipo) and optimized using full factorial, 3 experimental design. The optimized batch was then coated with chitosan to obtain CS-ERB Lipo and were characterized further. Both liposomal ERB formulations had size <200 nm and PDI < 0.4. Zeta potential was upto -50 mV for ERB Lipo and upto +25 mV for CS-ERB Lipo indicating stable formulation. Liposomal formulations were freeze dried and loaded into gel to study in-vitro release and chemotherapeutic evaluation. CS-ERB Lipo showed sustained release upto 36 h from gel as compared to control formulation. In-vitro cell viability studies showed potent anti-cancer activity on KB-cells. In-vivo studies showed better pharmacological efficacy in terms of tumor volume reduction for ERB Lipo gel (49.19%) and CS-ERB Lipo gel (55.27%) as compared to plain ERB Gel (38.88%) applied locally. Histology also revealed that formulation could alleviate dysplasia condition to hyperplasia. The locoregional therapy of ERB Lipo gel and CS-ERB Lipo gel thus show promising outcome in improving pre-malignant and early-stage oral cavity cancers.
口腔癌在全球范围内有超过 35 万例病例,其中 90%为口腔鳞状细胞癌(OSCC)。目前的放化疗治疗方法效果不佳,且对邻近的健康组织有有害影响。本研究旨在将厄洛替尼(ERB)局部递送至口腔中发生肿瘤的部位。ERB 被包裹在脂质体配方(ERB Lipo)中,并使用完全因子、3 实验设计进行优化。然后,用壳聚糖对优化后的批次进行包衣,得到 CS-ERB Lipo,并进一步进行了表征。两种脂质体 ERB 制剂的粒径均<200nm,PDI<0.4。ERB Lipo 的 zeta 电位高达-50mV,CS-ERB Lipo 的 zeta 电位高达+25mV,表明制剂稳定。脂质体制剂被冷冻干燥并装入凝胶中,以研究体外释放和化疗评价。CS-ERB Lipo 从凝胶中的释放可持续达 36 小时,而对照制剂则为 36 小时。体外细胞活力研究表明,KB 细胞对 ERB Lipo 凝胶(49.19%)和 CS-ERB Lipo 凝胶(55.27%)具有更强的抗癌活性,而与普通 ERB 凝胶(38.88%)相比。体内研究也表明,与普通 ERB 凝胶相比,ERB Lipo 凝胶(49.19%)和 CS-ERB Lipo 凝胶(55.27%)在局部应用时可更有效地减少肿瘤体积。组织学还表明,该制剂可缓解异型增生向增生的状况。因此,ERB Lipo 凝胶和 CS-ERB Lipo 凝胶的局部治疗在改善口腔癌前病变和早期口腔癌方面显示出有前景的结果。