Milk-derived exosomes for oral delivery of paclitaxel

被引:562
作者
Agrawal, Ashish K. [1 ]
Aqil, Farrukh [1 ,2 ]
Jeyabalan, Jeyaprakash [2 ]
Spencer, Wendy A. [3 ]
Beck, Joshua [3 ]
Gachuki, Beth W. [4 ,5 ]
Alhakeem, Sara S. [4 ,5 ]
Oben, Karine [4 ,5 ]
Munagala, Radha [1 ,2 ]
Bondada, Subbarao [4 ,5 ]
Gupta, Ramesh C. [1 ,3 ,6 ]
机构
[1] Univ Louisville, James Graham Brown Canc Ctr, Louisville, KY 40292 USA
[2] Univ Louisville, Dept Med, Louisville, KY 40292 USA
[3] 3P Biotechnol Inc, Louisville, KY USA
[4] Univ Kentucky, Dept Microbiol Immunol & Mol Genet, Lexington, KY USA
[5] Univ Kentucky, Markey Canc Ctr, Lexington, KY USA
[6] Univ Louisville, Dept Pharmacol & Toxicol, Louisville, KY 40292 USA
关键词
Exosomes; Taxol; Antitumor efficacy; Lung cancer; Systemic toxicity; Immunological responses; ENHANCED SOLUBILITY; BIOAVAILABILITY; NANOPARTICLES; CHEMOTHERAPY; STABILITY; LIPOSOMES;
D O I
10.1016/j.nano.2017.03.001
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
In this report milk-derived exosomes have been investigated for oral delivery of the chemotherapeutic drug paclitaxel (PAC) as an alternative to conventional i.v. therapy for improved efficacy and reduced toxicity. PAC-loaded exosomes (ExoPAC) were found to have a particle size of similar to 108 nm, a narrow particle size distribution (PDI similar to 0.190), zeta potential (similar to -7 mV) and a practical loading efficiency of similar to 8%. Exosomes and ExoPAC exhibited excellent stability in the presence of simulated-gastrointestinal fluids, and during the storage at -80 degrees C. A sustained release of PAC was also observed up to 48 h in vitro using PBS (pH 6.8). Importantly, ExoPAC delivered orally showed significant tumor growth inhibition (60%; P < 0.001) against human lung tumor xenografts in nude mice. Treatment with i.p. PAC at the same dose as ExoPAC, however, showed modest but statistically insignificant inhibition (31%). Moreover, ExoPAC demonstrated remarkably lower systemic and immunologic toxicities as compared to i.v. PAC. Published by Elsevier Inc.
引用
收藏
页码:1627 / 1636
页数:10
相关论文
共 38 条
[1]
Improved Stability and Antidiabetic Potential of Insulin Containing Folic Acid Functionalized Polymer Stabilized Multi layered Liposomes Following Oral Administration [J].
Agrawal, Ashish Kumar ;
Harde, Harshad ;
Thanki, Kaushik ;
Jain, Sanyog .
BIOMACROMOLECULES, 2014, 15 (01) :350-360
[2]
Overview of the changing paradigm in cancer treatment: Oral chemotherapy [J].
Aisner, Joseph .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2007, 64 :S4-S7
[3]
Exosomal formulation enhances therapeutic response of celastrol against lung cancer [J].
Aqil, Farrukh ;
Kausar, Hina ;
Agrawal, Ashish Kumar ;
Jeyabalan, Jeyaprakash ;
Kyakulaga, Al-Hassan ;
Munagala, Radha ;
Gupta, Ramesh .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2016, 101 (01) :12-21
[4]
Emerging nanopharmaceuticals [J].
Bawarski, Willie E. ;
Chidlowsky, Elena ;
Bharali, Dhruba J. ;
Mousa, Shaker A. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2008, 4 (04) :273-282
[5]
Beijnen JH, 1994, SEMIN ONCOL
[6]
PLGA Nanoparticles Stabilized with Cationic Surfactant: Safety Studies and Application in Oral Delivery of Paclitaxel to Treat Chemical-Induced Breast Cancer in Rat [J].
Bhardwaj, V. ;
Ankola, D. D. ;
Gupta, S. C. ;
Schneider, M. ;
Lehr, C. -M. ;
Kumar, M. N. V. Ravi .
PHARMACEUTICAL RESEARCH, 2009, 26 (11) :2495-2503
[7]
Chitosan coated layered clay montmorillonite nanocomposites modulate oral delivery of paclitaxel in colonic cancer [J].
Bothiraja, C. ;
Thorat, U. H. ;
Pawar, A. P. ;
Shaikh, K. S. .
MATERIALS TECHNOLOGY, 2014, 29 (B2) :B120-B126
[8]
Controlled Release, Intestinal Transport, and Oral Bioavailablity of Paclitaxel Can be Considerably Increased Using Suitably Tailored Pegylated Poly(Anhydride) Nanoparticles [J].
Calleja, Patricia ;
Espuelas, Socorro ;
Vauthier, Christine ;
Ponchel, Gilles ;
Irache, Juan M. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2015, 104 (09) :2877-2886
[9]
Acidity Generated by the Tumor Microenvironment Drives Local Invasion [J].
Estrella, Veronica ;
Chen, Tingan ;
Lloyd, Mark ;
Wojtkowiak, Jonathan ;
Cornnell, Heather H. ;
Ibrahim-Hashim, Arig ;
Bailey, Kate ;
Balagurunathan, Yoganand ;
Rothberg, Jennifer M. ;
Sloane, Bonnie F. ;
Johnson, Joseph ;
Gatenby, Robert A. ;
Gillies, Robert J. .
CANCER RESEARCH, 2013, 73 (05) :1524-1535
[10]
Successful mobilization of hematopoietic peripheral blood progenitor cells with paclitaxel-based chemotherapy as initial or salvage regimen in patients with hematologic malignancies [J].
Fernandez, Angel ;
De Arriba, Felipe ;
Rivera, Jose ;
Heras, Inmaculada ;
Vicente, Vicente ;
Luisa Lozano, Maria .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 (09) :1436-1438