Methotrexate Gold Nanocarriers: Loading and Release Study: Its Activity in Colon and Lung Cancer Cells

被引:31
作者
Alvarez-Gonzalez, Beatriz [1 ]
Rozalen, Marisa [1 ]
Fernandez-Perales, Maria [1 ]
Alvarez, Miguel A. [2 ]
Sanchez-Polo, Manuel [1 ]
机构
[1] Univ Granada, Fac Sci, Dept Inorgan Chem, Campus Fuentenueva S-N, Granada 18071, Spain
[2] Univ Jaen, Fac Sci, Dept Inorgan & Organ Chem, Campus Lagunillas S-N, Jaen 23071, Spain
关键词
Au nanoparticles; nanocarriers; methotrexate; anticancer drug; chemotherapeutics; controlled release; MAGNETIC NANOPARTICLES; DELIVERY; CARRIER; GROWTH; FOLATE; ACID; XPS;
D O I
10.3390/molecules25246049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, the synthesis of gold nanoparticles (AuNPs) loaded with methotrexate (MTX) has been carried out in order to obtain controlled size and monodispersed nanocarriers of around 20 nm. The characterization study shows metallic AuNPs with MTX polydispersed on the surface. MTX is linked by the replacement of citrate by the MTX carboxyl group. The drug release profiles show faster MTX release when it is conjugated, which leads to the best control of plasma concentration. Moreover, the enhanced release observed at pH 5 could take advantage of the pH gradients that exist in tumor microenvironments to achieve high local drug concentrations. AuNP-MTX conjugates were tested by flow cytometry against lung (A-549) and colon (HTC-116) cancer cell lines. Results for A-549 showed a weaker dose-response effect than for colon cancer ones. This could be related to the presence of folate receptors in line HTC-116 in comparison to line A-549, supporting the specific uptake of folate-conjugated AuNP-MTX by folate receptor positive tumor cells. Conjugates exhibited considerably higher cytotoxic effects compared with the effects of equal doses of free MTX. Annexin V-PI tests sustained the cell death mechanism of apoptosis, which is normally disabled in cancer cells.
引用
收藏
页数:18
相关论文
共 43 条
[1]   Gold nanoparticles in theranostic oncology: current state-of-the-art [J].
Akhter, Sohail ;
Ahmad, Mohammad Zaki ;
Ahmad, Farhan Jalees ;
Storm, Gert ;
Kok, Robbert J. .
EXPERT OPINION ON DRUG DELIVERY, 2012, 9 (10) :1225-1243
[2]  
Alexander MR, 1998, SURF INTERFACE ANAL, V26, P961, DOI 10.1002/(SICI)1096-9918(199812)26:13<961::AID-SIA432>3.0.CO
[3]  
2-7
[4]  
[Anonymous], 2014, Pharm. Technol. Eur
[5]   Gold nanoparticles: opportunities and challenges in nanomedicine [J].
Arvizo, Rochelle ;
Bhattacharya, Resham ;
Mukherjee, Priyabrata .
EXPERT OPINION ON DRUG DELIVERY, 2010, 7 (06) :753-763
[6]   Exploitation of intracellular pH gradients in the cellular delivery of macromolecules [J].
Asokan, A ;
Cho, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (04) :903-913
[7]   Molecular structure, vibrational spectra and DFT molecular orbital calculations (TD-DFT and NMR) of the antiproliferative drug Methotrexate [J].
Ayyappan, S. ;
Sundaraganesan, N. ;
Aroulmoji, V. ;
Murano, E. ;
Sebastian, S. .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2010, 77 (01) :264-275
[8]   Kinetically Controlled Seeded Growth Synthesis of Citrate-Stabilized Gold Nanoparticles of up to 200 nm: Size Focusing versus Ostwald Ripening [J].
Bastus, Neus G. ;
Comenge, Joan ;
Puntes, Victor .
LANGMUIR, 2011, 27 (17) :11098-11105
[9]   Functionalized gold nanoparticles for topical delivery of methotrexate for the possible treatment of psoriasis [J].
Bessar, Hagar ;
Venditti, Iole ;
Benassi, Luisa ;
Vaschieri, Cristina ;
Azzoni, Paola ;
Pellacani, Giovanni ;
Magnoni, Cristina ;
Botti, Elisabetta ;
Casagrande, Viviana ;
Federici, Massimo ;
Costanzo, Antonio ;
Fontana, Laura ;
Testa, Giovanna ;
Mostafa, Fawzia Farag ;
Ibrahim, Samia Ali ;
Russo, Maria Vittoria ;
Fratoddi, Ilaria .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2016, 141 :141-147
[10]  
BLEYER WA, 1978, CANCER-AM CANCER SOC, V41, P36, DOI 10.1002/1097-0142(197801)41:1<36::AID-CNCR2820410108>3.0.CO