Nagaraja Sreeharsha, Basavarajappa Girish Meravanige, Attimarad Mahesh, Pund Swati
Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Hofuf, Al-Ahsa 31982, Saudi Arabia.
Department of Pharmaceutics, Vidya Siri College of Pharmacy, Off Sarjapura Road, Bangalore 560035, Karnataka, India.
Pharmaceutics. 2021 Jun 18;13(6):902. doi: 10.3390/pharmaceutics13060902.
The present study is a mechanistic validation of 'proof-of-technology' for the effective topical delivery of chrysin nanoemulgel for localized, efficient treatment of melanoma-affected skin.
Currently available treatments for skin cancer are inefficient due to systemic side effects and poor transcutaneous permeation, thereby presenting a formidable challenge for the development of novel nanocarriers.
We opted for a novel approach and formulated a nanocomplex system composed of hydrophobic chrysin dissolved in a lipid mix, which was further nanoemulsified in Pluronic F-127 gel to enhance physicochemical and biopharmaceutic characteristics. Chrysin, a flavone extracted from passion flowers, exhibits potential anti-cancer activities; however, it has limited applicability due to its poor solubility. Pseudo-ternary phase diagrams were constructed to identify the best self-nanoemulsifying region by varying the compositions of oil, Caproyl 90 surfactant, Tween 80, and co-solvent Transcutol HP. Chrysin-loaded nanoemulsifying compositions were characterized for various physicochemical properties.
This thermodynamically stable, self-emulsifying drug delivery system showed a mean droplet size of 156.9 nm, polydispersity index of 0.26, and viscosity of 9100 cps after dispersion in gel. Mechanical characterization using Texture Analyzer exhibited that the gel had a hardness of 487 g and adhesiveness of 500 g. Ex vivo permeation through rat abdominal skin revealed significant improvement in percutaneous absorption measured as flux, the apparent permeability coefficient, the steady-state diffusion coefficient, and drug deposition. In vitro cytotoxicity on A375 and SK-MEL-2 cell lines showed a significantly improved therapeutic effect, thus ensuring reduction in dose. The safety of the product was established through biocompatibility testing on the L929 cell line.
Aqueous, gel-based, topical, nanoemulsified chrysin is a promising technology approach for effective localized transcutaneous delivery that will help reduce the frequency and overall dose usage and ultimately improve the therapeutic index.
本研究是对“技术验证”的机制性验证,该验证用于将白杨素纳米乳凝胶有效局部递送至受黑色素瘤影响的皮肤,进行局部高效治疗。
由于全身副作用和经皮渗透不良,目前可用的皮肤癌治疗方法效率低下,这对新型纳米载体的开发提出了巨大挑战。
我们选择了一种新颖的方法,制备了一种纳米复合体系,该体系由溶解在脂质混合物中的疏水性白杨素组成,然后在普朗尼克F - 127凝胶中进一步纳米乳化,以增强其物理化学和生物药剂学特性。白杨素是从西番莲中提取的一种黄酮,具有潜在的抗癌活性;然而,由于其溶解度差,其应用有限。通过改变油、己酰90表面活性剂、吐温80和助溶剂二甲基亚砜的组成构建伪三元相图,以确定最佳的自纳米乳化区域。对负载白杨素的纳米乳化组合物的各种物理化学性质进行了表征。
这种热力学稳定的自乳化药物递送系统在分散于凝胶后,平均液滴尺寸为156.9 nm,多分散指数为0.26,粘度为9100 cps。使用质构分析仪进行的力学表征显示,该凝胶的硬度为487 g,粘附性为500 g。通过大鼠腹部皮肤的离体渗透显示,以通量、表观渗透系数、稳态扩散系数和药物沉积衡量的经皮吸收有显著改善。对A375和SK - MEL - 2细胞系的体外细胞毒性显示治疗效果显著改善,从而确保了剂量的减少。通过对L929细胞系的生物相容性测试确定了该产品的安全性。
水性、基于凝胶的局部纳米乳化白杨素是一种有前景的技术方法,可实现有效的局部经皮递送,这将有助于减少给药频率和总体剂量使用,并最终提高治疗指数。