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新型基于胶凝多糖的原位纳米囊泡制剂的多西他赛局部递送——利用储库形成作用

Novel Gellan Gum-Based In Situ Nanovesicle Formulation of Docetaxel for Its Localized Delivery Using Depot Formation.

机构信息

Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, 143005, India.

Department of Food Science and Technology, Guru Nanak Dev University, Amritsar, 143005, India.

出版信息

AAPS PharmSciTech. 2021 May 27;22(5):165. doi: 10.1208/s12249-021-02033-7.

Abstract

In the present study, different in situ hydrogel formulations of docetaxel (DTX) based on biocompatible polymers such as Hyaluronic Acid (HA), poloxamer-407, chitosan and gellan gum were formulated to increase its therapeutic efficacy and reduce toxicity. DTX was loaded in nanovesicles (20 mg/mL equivalent to commercial strength) and further incorporated into the hydrogel bases to possess a dual rationale of protection against burst release and enhanced solubility of the drug. The optimized hydrogel formulation (NV-TPGS-3-GG-4) showed ideal rheological behavior and in situ characteristics at 37±0.5°C with sustained release of more than 144 h. The optimized formulation had instant in vitro gelation (2.8±0.3 min) with good injectability in comparison to the conventional commercial DTX injectable formulation having instant release (<2 h). Additionally, developed formulation exhibited an improved biodisponibility (25.1±0.2 h) in comparison to the commercially available formulation (1.7±0.1 h). The Solid Tumor Carcinoma model in Swiss albino mice revealed that the optimized formulation (based on gellan gum) showed better tumor reduction (85.7±1.2%) and lower toxicity as compared to the commercial formulation (77.3±1.3%). Pharmacokinetic and biodistribution studies demonstrated 3 to 4 times higher localization of drug in tumors. Our findings suggested that injectable gellan gum-based in situ hydrogel formulation can be an effective delivery system for DTX with enhanced solubility, reduced toxicity, and better targeting to the tumors for improved therapeutics.Graphical abstract.

摘要

在本研究中,基于生物相容性聚合物(如透明质酸 (HA)、泊洛沙姆 407、壳聚糖和结冷胶),我们设计了不同的多西紫杉醇(DTX)原位水凝胶制剂,以提高其治疗效果并降低毒性。将 DTX 负载到纳米囊泡中(20mg/mL 相当于商业强度),并进一步掺入水凝胶基质中,具有防止药物突释和提高药物溶解度的双重原理。优化的水凝胶制剂(NV-TPGS-3-GG-4)在 37±0.5°C 下表现出理想的流变行为和原位特性,药物释放可持续超过 144 小时。与具有即时释放(<2 小时)的常规商业 DTX 注射液相比,优化的制剂具有即时体外凝胶化(2.8±0.3 分钟)和良好的可注射性。此外,与市售制剂(1.7±0.1 小时)相比,所开发的制剂表现出更好的生物利用度(25.1±0.2 小时)。在瑞士白化病小鼠的实体瘤癌模型中,优化的制剂(基于结冷胶)显示出更好的肿瘤缩小(85.7±1.2%)和更低的毒性,与商业制剂(77.3±1.3%)相比。药代动力学和生物分布研究表明,药物在肿瘤中的定位提高了 3 至 4 倍。我们的研究结果表明,基于结冷胶的可注射原位水凝胶制剂可作为 DTX 的有效给药系统,具有提高的溶解度、降低的毒性和更好的肿瘤靶向性,从而改善治疗效果。

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