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2
Novel diindolylmethane derivatives based NLC formulations to improve the oral bioavailability and anticancer effects in triple negative breast cancer.基于新型二吲哚甲烷衍生物的纳米脂质载体配方可提高三阴性乳腺癌的口服生物利用度和抗癌效果。
Eur J Pharm Biopharm. 2016 Nov;108:168-179. doi: 10.1016/j.ejpb.2016.08.006. Epub 2016 Aug 30.
3
Quercetin-loaded freeze-dried nanomicelles: Improving absorption and anti-glioma efficiency in vitro and in vivo.槲皮素载冷冻干燥纳米胶束:提高体外和体内的吸收和抗脑胶质瘤效率。
J Control Release. 2016 Aug 10;235:276-290. doi: 10.1016/j.jconrel.2016.05.045. Epub 2016 May 27.
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Noscapine chemosensitization enhances docetaxel anticancer activity and nanocarrier uptake in triple negative breast cancer.那可丁化学增敏作用增强了多西他赛在三阴性乳腺癌中的抗癌活性及纳米载体摄取。
Exp Cell Res. 2016 Aug 1;346(1):65-73. doi: 10.1016/j.yexcr.2016.05.006. Epub 2016 May 10.
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Tumor stromal disrupting agent enhances the anticancer efficacy of docetaxel loaded PEGylated liposomes in lung cancer.肿瘤基质破坏剂增强了载多西他赛的聚乙二醇化脂质体在肺癌中的抗癌疗效。
Nanomedicine (Lond). 2016 Jun;11(11):1377-92. doi: 10.2217/nnm.16.37. Epub 2016 May 12.
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Honokiol protects against renal ischemia/reperfusion injury via the suppression of oxidative stress, iNOS, inflammation and STAT3 in rats.和厚朴酚通过抑制氧化应激、iNOS、炎症和 STAT3 来防止大鼠肾缺血再灌注损伤。
Mol Med Rep. 2016 Feb;13(2):1353-60. doi: 10.3892/mmr.2015.4660. Epub 2015 Dec 9.
9
Sirolimus-loaded polymeric micelles with honokiol for oral delivery.负载西罗莫司并含有厚朴酚的聚合物胶束用于口服给药。
J Pharm Pharmacol. 2015 Dec;67(12):1663-72. doi: 10.1111/jphp.12482. Epub 2015 Oct 10.
10
Piperlongumine for Enhancing Oral Bioavailability and Cytotoxicity of Docetaxel in Triple-Negative Breast Cancer.胡椒碱增强多西他赛在三阴性乳腺癌中的口服生物利用度和细胞毒性
J Pharm Sci. 2015 Dec;104(12):4417-4426. doi: 10.1002/jps.24637. Epub 2015 Sep 15.

厚朴酚纳米胶束制剂提高了三阴性乳腺癌(TNBC)的口服生物利用度和抗癌效果。

Honokiol nanomicellar formulation produced increased oral bioavailability and anticancer effects in triple negative breast cancer (TNBC).

作者信息

Godugu Chandraiah, Doddapaneni Ravi, Singh Mandip

机构信息

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.

出版信息

Colloids Surf B Biointerfaces. 2017 May 1;153:208-219. doi: 10.1016/j.colsurfb.2017.01.038. Epub 2017 Jan 23.

DOI:10.1016/j.colsurfb.2017.01.038
PMID:28249200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5745346/
Abstract

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.

摘要

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。