Inhalable spray dried lipidnanoparticles for the co-delivery of paclitaxel and doxorubicin in lung cancer

被引:30
作者
Kaur, Prabhjot [1 ]
Mishra, Vijay [1 ]
Shunmugaperumal, Tamilvanan [2 ]
Goyal, Amit K. [3 ]
Ghosh, Goutam [4 ]
Rath, Goutam [4 ]
机构
[1] Lovely Profess Univ, Jalandhar, Punjab, India
[2] Natl Inst Pharmaceut Educ & Res NIPER Guwahati, Dept Pharmaceut, Gauhati, Assam, India
[3] Cent Univ Rajasthan, Ajmer, Rajasthan, India
[4] Siksha OAnusandhan, Bhubaneswar, Odisha, India
关键词
Surfactant; Anticancer drugs; Nanolipid carrier; Inhalable nanoaggregates; Lung cancer; EFFLUX TRANSPORTER ACTIVITY; SOLID LIPID NANOPARTICLES; P-GLYCOPROTEIN; PHARMACEUTICAL EXCIPIENTS; POLY(ETHYLENE GLYCOL); CACO-2; CELLS; SURFACTANTS; NANOMEDICINE; ABSORPTION; SECRETION;
D O I
10.1016/j.jddst.2020.101502
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study aimed to develop and evaluate inhalable nanocarriers using different surfactants for enhancing the antitumor efficacy of chemotherapeutics. Surfactants (Cremophor EL, Tween 80 and Tween 20) loaded nano-lipid carriers (NLCs) containing Paclitaxel (PTX) and Doxorubicin (DOX) were prepared through solvent evaporation followed by spray drying technique. The prepared inhalable nanoaggregates were evaluated for various pharmaceutical and aerodynamic properties. Animal model was used to determine in-vivo drug distribution, and safety profile of optimized formulations. Particle size distribution analysis indicated that Cremophor EL based nanocarriers have smallest particle size distribution (394.1 +/- 5.6 nm) compared to Tween 80 and Tween 20 characterized by size values, 575.6 +/- 3.3 nm and 460.7 +/- 2.6 nm, respectively. DSCand XRD analysis show no characteristic change in solid state properties of drugs in optimized formulation. Organ distribution studies demonstrated Cremophor EL DPIs show higher drug distribution in the lungs compared to other experimental formulations and plain drugs. Further animals treated with experimental DPIs show no sign of tissue damage with usual feeding and drinking behaviour after 24 h of treatment. In this study, spray-dried nanoaggregates composed of Cremophor EL encapsulating PTX and DOX offer a possible strategy to reverse the growing concern of drug resistance for improved therapeutic adherence.
引用
收藏
页数:10
相关论文
共 27 条
[1]   Optimal structure requirements for pluronic block copolymers in modifying P-glycoprotein drug efflux transporter activity in bovine brain microvessel endothelial cells [J].
Batrakova, EV ;
Li, S ;
Alakhov, VY ;
Miller, DW ;
Kabanov, AV .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (02) :845-854
[2]   Role of P-glycoprotein as a secretory mechanism in quinidine absorption from rat small intestine [J].
Emi, Y ;
Tsunashima, D ;
Ogawara, K ;
Higaki, K ;
Kimura, T .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (03) :295-299
[3]   Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 [J].
Ferlay, Jacques ;
Soerjomataram, Isabelle ;
Dikshit, Rajesh ;
Eser, Sultan ;
Mathers, Colin ;
Rebelo, Marise ;
Parkin, Donald Maxwell ;
Forman, David ;
Bray, Freddie .
INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (05) :E359-E386
[4]  
Finlay WH, 2019, MECHANICS OF INHALED PHARMACEUTICAL AEROSOLS: AN INTRODUCTION, P1, DOI 10.1016/B978-0-12-256971-5.X5000-7
[5]   Characterization of the A549 cell line as a type II pulmonary epithelial cell model for drug metabolism [J].
Foster, KA ;
Oster, CG ;
Mayer, MM ;
Avery, ML ;
Audus, KL .
EXPERIMENTAL CELL RESEARCH, 1998, 243 (02) :359-366
[6]   IN-VITRO CULTIVATION OF HUMAN TUMORS - ESTABLISHMENT OF CELL LINES DERIVED FROM A SERIES OF SOLID TUMORS [J].
GIARD, DJ ;
AARONSON, SA ;
TODARO, GJ ;
ARNSTEIN, P ;
KERSEY, JH ;
DOSIK, H ;
PARKS, WP .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1973, 51 (05) :1417-1423
[7]   The applications of Vitamin E TPGS in drug delivery [J].
Guo, Yuanyuan ;
Luo, Jun ;
Tan, Songwei ;
Otieno, Ben Oketch ;
Zhang, Zhiping .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 49 (02) :175-186
[8]   Effects of poly(ethylene glycol) on efflux transporter activity in Caco-2 cell monolayers [J].
Hugger, ED ;
Audus, KL ;
Borchardt, RT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (09) :1980-1990
[9]   A comparison of commonly used polyethoxylated pharmaceutical excipients on their ability to inhibit P-glycoprotein activity in vitro [J].
Hugger, ED ;
Novak, BL ;
Burton, PS ;
Audus, KL ;
Borchardt, RT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (09) :1991-2002
[10]   Intestinal secretion of drugs. The role of P-glycoprotein and related drug efflux systems in limiting oral drug absorption [J].
Hunter, J ;
Hirst, BH .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 25 (2-3) :129-157