Disha Nagesh Moholkar, Raghuram Kandimalla, Jeyaprakash Jeyabalan, Jun Yan, Zhao-Hui Song, Farrukh Aqil, Ramesh C. Gupta
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Cell culture assays (MTT, colony forming) are performed to analyze the anti-cancer activity of CBD and ExoCBD against drug-sensitive and resistant lung cancer cells and followed by orthotopic lung tumor xenograft mouse-model. FA-functionalized exosomal formulation of CBD provides a drug load of 20–24%. CBD and its exosomal formulations show antiproliferative and anti-inflammatory activities against both lung cancer cells and reduce the colony forming ability. Mechanistically, CBD decreased the expression of CB2, cell cycle markers, NF-κB, and IκBα, while increasing GPR3 levels in both drug-sensitive and drug-resistant lung cancer cells, as well as MDR-1 in drug-resistant cells. Orally administered FA-ExoCBD shows superior tumor growth inhibition as compared to free CBD (80% vs 60%) at one-half the dose of 7.5 mg kg<sup>−1</sup> versus 15 mg kg<sup>−1</sup>. 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引用次数: 0
摘要
尽管肺癌的治疗取得了进展,但由于缺乏特异性和选择性,生存率仍然很低。使用合适的纳米给药载体可以克服这些问题。大麻二酚(CBD)有潜力成为一种新型的治疗癌症的药物。该研究利用初乳衍生的外泌体作为纳米载体来递送CBD,以克服其低口服生物利用度。外泌体是通过连续的超离心从初乳粉中分离出来的。在CBD加载后,配方(ExoCBD和FA-ExoCBD)的物理参数(大小、电荷和zeta电位)被表征。细胞培养实验(MTT,集落形成)分析CBD和ExoCBD对药物敏感和耐药肺癌细胞的抗癌活性,然后进行原位肺肿瘤异种移植小鼠模型。fa功能化的CBD外泌体制剂提供20-24%的药物负荷。CBD及其外泌体制剂对肺癌细胞具有抗增殖和抗炎活性,并降低集落形成能力。在机制上,CBD降低了CB2、细胞周期标志物、NF-κB和i -κB α的表达,同时增加了药敏和耐药肺癌细胞中GPR3的表达,以及耐药细胞中MDR-1的表达。与游离CBD相比,口服FA-ExoCBD在7.5 mg kg - 1和15 mg kg - 1的一半剂量下显示出更好的肿瘤生长抑制作用(80% vs 60%)。FA-ExoCBD可作为一种潜在的靶向口服药物用于肺癌的治疗。
Targeted Oral Delivery of Exosomal Formulation of Cannabidiol against Lung Cancer
Despite advances in the treatment of lung cancer, the survival rate remains low due to lack of specificity and selectivity. The use of appropriate nano-drug delivery vehicle can overcome these issues. Cannabidiol (CBD) has the potential to be used as a novel therapeutic agent for treating cancer. The study utilizes colostrum-derived exosomes as nano-carriers for the delivery of CBD to overcome its low oral bioavailability. Exosomes are isolated from colostrum powder by sequential ultracentrifugation. Following CBD loading the formulations (ExoCBD and FA-ExoCBD) are characterized for their physical parameters (size, charge, and zeta potential). Cell culture assays (MTT, colony forming) are performed to analyze the anti-cancer activity of CBD and ExoCBD against drug-sensitive and resistant lung cancer cells and followed by orthotopic lung tumor xenograft mouse-model. FA-functionalized exosomal formulation of CBD provides a drug load of 20–24%. CBD and its exosomal formulations show antiproliferative and anti-inflammatory activities against both lung cancer cells and reduce the colony forming ability. Mechanistically, CBD decreased the expression of CB2, cell cycle markers, NF-κB, and IκBα, while increasing GPR3 levels in both drug-sensitive and drug-resistant lung cancer cells, as well as MDR-1 in drug-resistant cells. Orally administered FA-ExoCBD shows superior tumor growth inhibition as compared to free CBD (80% vs 60%) at one-half the dose of 7.5 mg kg−1 versus 15 mg kg−1. FA-ExoCBD can be developed as a potential targeted oral drug in the quest of lung cancer management.