Godugu Chandraiah, Doddapaneni Ravi, Singh Mandip
College of Pharmacy Pharmaceutical Sciences, Florida A & M University, Tallahassee, FL 32307, USA; Department of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research, Balanagar, Hyderabad, Telangana 500037 India.
College of Pharmacy Pharmaceutical Sciences, Florida A & M University, Tallahassee, FL 32307, USA; Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Colloids Surf B Biointerfaces. 2017 May 1;153:208-219. doi: 10.1016/j.colsurfb.2017.01.038. Epub 2017 Jan 23.
Triple negative breast cancer (TNBC), owing to its aggressive behavior and toxicity associated with available chemotherapy; currently no suitable therapy is available. Honokiol (HNK) is a promising anticancer drug but has poor bioavailability. In the current study, we evaluated the anticancer effects of an oral Honokiol nanomicellar (NM) formulation (size range of 20-40nm) in vitro against various TNBC cells lines. Cytotoxicity, clonogenic and wound healing assays demonstrated the promising anticancer effects. In vitro Caco-2 permeability studies suggested increased absorption of Honokiol. Compared to HNK-FD, nanomicellar formulations resulted in significant increase in the oral bioavailability. C (4.06 and 3.60-fold) and AUC (6.26 and 5.83-fold) were significantly increased in comparison to oral 40 and 80mg/kg free drug respectively. Further, anticancer effects of these formulations were studied in BALB/c nude mice transplanted with orthotopic MDA-MB-231 cell induced xenografts. After 4 weeks of daily administration of HNK-NM formulation, significant reduction in the tumor volumes and weights compared to free drug (p<0.001) treated groups was observed. Surprisingly, in some of the animals (25%), the treatment resulted in complete eradication of tumors. Increased apoptosis and antiangiogenic effect was observed in HNK-NM groups compared to free drug and untreated control animals. This is the first report demonstrating that HNK-FD possesses anticancer effects against TNBC.
三阴性乳腺癌(TNBC)因其侵袭性以及与现有化疗相关的毒性,目前尚无合适的治疗方法。厚朴酚(HNK)是一种有前景的抗癌药物,但生物利用度较差。在本研究中,我们评估了口服厚朴酚纳米胶束(NM)制剂(尺寸范围为20 - 40nm)在体外对各种三阴性乳腺癌细胞系的抗癌作用。细胞毒性、克隆形成和伤口愈合试验证明了其有前景的抗癌效果。体外Caco - 2通透性研究表明厚朴酚的吸收增加。与厚朴酚游离药物(HNK - FD)相比,纳米胶束制剂使口服生物利用度显著提高。与口服40mg/kg和80mg/kg游离药物相比,纳米胶束制剂的血药浓度(分别提高4.06倍和3.60倍)和药时曲线下面积(分别提高6.26倍和5.83倍)显著增加。此外,在移植了原位MDA - MB - 231细胞诱导异种移植瘤的BALB/c裸鼠中研究了这些制剂的抗癌作用。在每日给予厚朴酚纳米胶束制剂4周后,与游离药物治疗组相比,观察到肿瘤体积和重量显著减小(p<0.001)。令人惊讶的是,在一些动物(25%)中,治疗导致肿瘤完全消除。与游离药物组和未治疗的对照动物相比,厚朴酚纳米胶束组观察到凋亡增加和抗血管生成作用。这是首次报道表明厚朴酚游离药物对三阴性乳腺癌具有抗癌作用。