Co-Loading of Cisplatin and Methotrexate in Nanoparticle-Based PCL-PEG System Enhances Lung Cancer Chemotherapy Effects

被引:17
作者
Akbari, Elahe [1 ,6 ]
Mousazadeh, Hanieh [1 ]
Hanifehpour, Younes [2 ]
Mostafavi, Ebrahim [3 ]
Gorabi, Armita Mahdavi [11 ]
Nejati, Kazem [8 ]
Keyhanvar, Peyman [4 ]
Pazoki-Toroudi, Hamidreza [9 ,10 ]
Mohammadhosseini, Majid [7 ]
Akbarzadeh, Abolfazl [4 ,5 ]
机构
[1] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Biotechnol, Tabriz, Iran
[2] Sayyed Jamaleddin Asadabadi Univ, Dept Chem, Asadabad, Iran
[3] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
[4] Tabriz Univ Med Sci, Stem Cell Res Ctr, Tabriz, Iran
[5] Universal Sci Educ & Res Network USERN, Tabriz, Iran
[6] Higher Educ Inst Rab Rashid, Tabriz, Iran
[7] Islamic Azad Univ, Dept Chem, Shahrood Branch, Shahrood, Iran
[8] Ardabil Univ Med Sci, Pharmaceut Sci Res Ctr, Ardebil, Iran
[9] Iran Univ Med Sci, Fac Med, Physiol Res Ctr, Tehran, Iran
[10] Iran Univ Med Sci, Fac Med, Dept Physiol, Tehran, Iran
[11] Univ Tehran Med Sci, Endocrinol & Metab Populat Sci Inst, Chron Dis Res Ctr, Tehran, Iran
关键词
Cisplatin (CDDP); Methotrexate (MTX); Poly(E-caprolactone) (PCL); Nanoparticles; Lung cancer; COMBINATION CHEMOTHERAPY; DOWN-REGULATION; P-GLYCOPROTEIN; CELL; CARCINOMA; THERAPY; CYTOTOXICITY; EXPRESSION; MANAGEMENT; DOCETAXEL;
D O I
10.1007/s10876-021-02101-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Since the anticancer drugs exhibited a variety of inhibitory mechanisms in cancer cells, the use of two or more anticancer drugs may have excellent therapeutic effects, particularly in drug-resistant tumors. In this study, the efficient entrapment of two clinically used single-agent drugs, Cisplatin (CDDP) and Methotrexate (MTX) is reported against lung cancer cell lines. Biodegradable polymeric nanoparticles perform to be a favorable environment-responsive controlled drug release system. MTX@CDDP were simultaneously encapsulated into the biodegradable poly (epsilon-caprolactone) (PCL) modified poly (ethylene glycol) (PEG) copolymer. The spherical nanoparticle was identified via scanning electron microscopy (SEM). Additionally, the antitumor activity and apoptosis induction of designed duel drug-loaded vectors were assessed against A549 cell lines by qRT-PCR, MTT assay, and DAPI staining. The nanoformulation loaded with MTX@CDDP statistically reduced the cell activity of A549. The results indicate that MTX@CDDP-loaded PCL-PEG nanoparticles can be further utilized for treating non-small-cell lung cancer as a promising therapeutic approach. [GRAPHICS] .
引用
收藏
页码:1751 / 1762
页数:12
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