Development of an in-situ forming implant system for levodopa and carbidopa for the treatment of parkinson's disease.

IF 5.7 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Deepa D Nakmode, Sadikalmahdi Abdella, Yunmei Song, Sanjay Garg
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引用次数: 0

Abstract

Long-acting injectables have gained attraction as a system for treating chronic conditions due to their increased efficacy, safety, and patient compliance. Currently, patients with Parkinsons need to administer oral medications multiple times a day which imposes the significant risk of non-compliance. This study aimed to design an in-situ implant-forming system for controlled delivery of levodopa and carbidopa for up to 1 week which will reduce the need for multiple dosing. The combination of poly-lactic-co-glycolic acid (PLGA 50:50) and Eudragit L-100 was used to prepare the implants and the formulation was optimized to achieve a controlled release over 7 days. The optimized formulation containing 26% PLGA and 6% Eudragit L 100 displayed a favorable release profile and injectability with low viscosity. The optimized formulation in vitro release study revealed an initial burst of 34.17% and 37.16% for levodopa and carbidopa in the first 24 h and about 92% and 81% release within 7 days. A good correlation was observed between the in-vitro drug release data and ex-vivo drug release with a correlation coefficient of 0.91 for levodopa and 0.90 for carbidopa. Viscosity analysis showed the Newtonian behavior of the formulation. Syringeability analysis of the formulation showed that the maximum force required for expelling the formulation was 32.98 ± 0.72 N using a 22 G needle. The in-vitro degradation studies revealed 81.89% weight loss of implant in 7 days. The prepared formulation was assessed for in-vivo performance using a convolution modeling technique using a convolve function in R software. The predicted AUC 0-∞ h for the in-situ forming implant was 26505.5 ng/ml with Cmax, 399.3 ng/ml, and Tmax 24 h assuming 100% bioavailability. The results justify that the prepared in-situ implant forming system can be a promising system for the delivery of levodopa and carbidopa for Parkinson's patients.

用于治疗帕金森病的左旋多巴和卡比多巴原位成形植入系统的研制。
长效注射剂由于其更高的疗效、安全性和患者依从性,作为一种治疗慢性疾病的系统已经获得了吸引力。目前,帕金森氏症患者需要每天服用多次口服药物,这带来了很大的不依从性风险。本研究旨在设计一种原位植入成型系统,用于控制左旋多巴和卡比多巴长达1周的给药,以减少多次给药的需要。采用聚乳酸-羟基乙酸(PLGA: 50:50)与Eudragit L-100联合制备植入物,优化配方,达到7 d控释。优化后的配方含有26%的PLGA和6%的Eudragit l100,具有良好的释放特性和低粘度的注射性。优化后的制剂体外释放度研究表明,左旋多巴和卡比多巴在24 h内的初始释放量分别为34.17%和37.16%,7 d内的释放量分别为92%和81%。左旋多巴的体外释放量与体外释放量具有良好的相关性,相关系数为0.91,卡比多巴为0.90。粘度分析显示了该配方的牛顿行为。注射性分析表明,使用22 G针,排出该制剂所需的最大作用力为32.98±0.72 N。体外降解研究显示,7天内种植体重量减轻81.89%。在R软件中使用卷积函数使用卷积建模技术评估制备的制剂的体内性能。假设100%生物利用度,原位成形植入物的AUC 0-∞h为26505.5 ng/ml, Cmax为399.3 ng/ml, Tmax为24 h。结果表明,所制备的原位植入物形成系统可以作为帕金森病患者左旋多巴和卡比多巴的输送系统。
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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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