Co-delivery of cisplatin and siRNA through hybrid nanocarrier platform for masking resistance to chemotherapy in lung cancer

被引:25
作者
Patel, Vivek [1 ]
Lalani, Rohan [1 ]
Vhora, Imran [1 ]
Bardoliwala, Denish [1 ]
Patel, Akanksha [1 ]
Ghosh, Saikat [1 ]
Misra, Ambikanandan [1 ,2 ]
机构
[1] Maharaja Sayajirao Univ Baroda, Fac Pharm, Dept Pharmaceut, Kalabhavan Campus, Vadodara 390001, Gujarat, India
[2] SVKMs NMIMS Univ, Shobhaben Pratapbhai Patel Sch Pharm & Technol Ma, Mumbai 400056, Maharashtra, India
关键词
Cisplatin; Lung cancer; Nanocarrier; Resistance; Simultaneous; siRNA; IN-VITRO; MULTIDRUG-RESISTANCE; DRUG-DELIVERY; NANOPARTICLES; PEG; GEMCITABINE; PACLITAXEL; LIPOSOMES; SURFACE; SHELL;
D O I
10.1007/s13346-020-00867-5
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The resistance of cancer cells to chemotherapy has presented a formidable challenge. The current research aims at evaluating whether silencing of the cisplatin efflux promoter gene ABCC3 using siRNA co-loaded with the drug in a nanocarrier improves its efficacy in non-small cell lung cancer (NSCLC). Hybrid nanocarriers (HNCs) comprising lipids and poly(lactic acid-polyethylene glycol) di-block copolymer (PEG-PLA) were prepared for achieving the simultaneous delivery of cisplatin caprylate and ABCC3-siRNA to the cancer cells. PEGylation of the formulated HNCs was carried out using post-insertion technique for imparting long circulation characteristics to the carrier. The optimized formulation exhibited an entrapment efficiency of 71.9 +/- 2.2% and 95.83 +/- 0.39% for cisplatin caprylate and siRNA respectively. Further, the HNC was found to have hydrodynamic diameter of 153.2 +/- 1.76 nm and + 25.39 +/- 0.49 mV zeta potential. Morphological evaluation using cryo transmission electron microscopy confirmed the presence of lipid bilayer surrounding the polymeric core in HNCs. The in vitro cellular uptake studies showed improved uptake, while cell viability studies of the co-loaded formulation in A549 cell-line indicated significantly improved cytotoxic potential when compared with drug solution and drug-loaded HNCs; cell cycle analysis indicated increased percentage of cell arrest in G2-M phase compared with drug-loaded HNCs. Further, the gene knock-down study showed that silencing of ABCC3 mRNA might be improved in vitro efficacy of the formulation. The optimized cisplatin and ABCC3 siRNA co-loaded formulation presented significantly increased half-life and tumour regression in A549 xenograft model in BALB/c nude mice. In conclusion, siRNA co-loaded formulation presented reduced drug resistance and increased efficacy, which might be promising for the current cisplatin-based treatments in NSCLC.
引用
收藏
页码:2052 / 2071
页数:20
相关论文
共 57 条
[1]   Nanotoxicology and in vitro studies: The need of the hour [J].
Arora, Sumit ;
Rajwade, Jyutika M. ;
Paknikar, Kishore M. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2012, 258 (02) :151-165
[2]   Nanocarriers in effective pulmonary delivery of siRNA: current approaches and challenges [J].
Bardoliwala, Denish ;
Patel, Vivek ;
Javia, Ankit ;
Ghosh, Saikat ;
Patel, Akanksha ;
Misra, Ambikanandan .
THERAPEUTIC DELIVERY, 2019, 10 (05) :311-332
[3]   RRM1 modulated in vitro and in vivo efficacy of gemcitabine and platinum in non-small-cell lung cancer [J].
Bepler, Gerold ;
Kusmartseva, Irina ;
Sharma, Swati ;
Gautam, Ashish ;
Cantor, Alan ;
Sharma, Anupama ;
Simon, George .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (29) :4731-4737
[4]   An in vitro Assessment of Thermo-Reversible Gel Formulation Containing Sunitinib Nanoparticles for Neovascular Age-Related Macular Degeneration [J].
Bhatt, Priyanka ;
Narvekar, Priya ;
Lalani, Rohan ;
Chougule, Mahavir Bhupal ;
Pathak, Yashwant ;
Sutariya, Vijaykumar .
AAPS PHARMSCITECH, 2019, 20 (07)
[5]   Liposomes encapsulating native and cyclodextrin enclosed paclitaxel: Enhanced loading efficiency and its pharmacokinetic evaluation [J].
Bhatt, Priyanka ;
Lalani, Rohan ;
Vhora, Imran ;
Patil, Sushilkumar ;
Amrutiya, Jitendra ;
Misra, Ambikanandan ;
Mashru, Rajashree .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 536 (01) :95-107
[6]   Principles of nanoparticle design for overcoming biological barriers to drug delivery [J].
Blanco, Elvin ;
Shen, Haifa ;
Ferrari, Mauro .
NATURE BIOTECHNOLOGY, 2015, 33 (09) :941-951
[7]   PLGA-lecithin-PEG core-shell nanoparticles for controlled drug delivery [J].
Chan, Juliana M. ;
Zhang, Liangfang ;
Yuet, Kai P. ;
Liao, Grace ;
Rhee, June-Wha ;
Langer, Robert ;
Farokhzad, Omid C. .
BIOMATERIALS, 2009, 30 (08) :1627-1634
[8]  
Chen BA, 2010, INT J NANOMED, V5, P437
[9]   An efficient and low immunostimulatory nanoparticle formulation for systemic siRNA delivery to the tumor [J].
Chono, Sumio ;
Li, Shyh-Dar ;
Conwell, Christine C. ;
Huang, Leaf .
JOURNAL OF CONTROLLED RELEASE, 2008, 131 (01) :64-69
[10]   Co-delivery of siRNA and therapeutic agents using nanocarriers to overcome cancer resistance [J].
Creixell, Mar ;
Peppas, Nicholas A. .
NANO TODAY, 2012, 7 (04) :367-379