Transferrin-Conjugated PLGA Nanoparticles for Co-Delivery of Temozolomide and Bortezomib to Glioblastoma Cells

被引:16
|
作者
Ramalho, Maria Joao [1 ,2 ]
Torres, Ines David [1 ,2 ]
Loureiro, Joana Angelica [1 ,2 ]
Lima, Jorge [3 ,4 ,5 ]
Pereira, Maria Carmo [1 ,2 ]
机构
[1] Univ Porto, Fac Engn, LEPABE Lab Proc Engn Environm Biotechnol & Energy, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[2] Univ Porto, Fac Engn, ALiCE Associate Lab Chem Engn, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[3] Univ Porto, i3S Inst Invest & Inovacao Saude, R Alfredo Allen, P-420010135 Porto, Portugal
[4] Univ Porto, Ipatimup Inst Patol & Imunol Mol, Rua Julio Amaral de Carvalho 45, P-4200135 Porto, Portugal
[5] Univ Porto, Fac Med, Alameda Prof Hernani Monteiro, P-4200319 Porto, Portugal
基金
欧盟地平线“2020”;
关键词
high-grade glioma; brain tumor; MGMT protein; drug resistance mechanisms; alkylatingagents; poly(lactic-co-glycolic acid); brain delivery; transferrin receptor; METHYLTRANSFERASE MGMT; IRON-BINDING; RELEASE; BRAIN; DOXORUBICIN; INHIBITION; INCREASES; PROMOTER;
D O I
10.1021/acsanm.3c02122
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Glioblastoma (GBM)represents almost half of primarybrain tumors,and its standard treatment with the alkylating agent temozolomide(TMZ) is not curative. Treatment failure is partially related to intrinsicresistance mechanisms mediated by the O6-methylguanine-DNA methyltransferase(MGMT) protein, frequently overexpressed in GBM patients. Clinicaltrials have shown that the anticancer agent bortezomib (BTZ) can increaseTMZ's therapeutic efficacy in GBM patients by downregulatingMGMT expression. However, the clinical application of this therapeuticstrategy has been stalled due to the high toxicity of the combinedtherapy. The co-delivery of TMZ and BTZ through nanoparticles (NPs)of poly(lactic-co-glycolic acid) (PLGA) is proposedin this work, aiming to explore their synergistic effect while decreasingthe drug's toxicity. The developed NPs were optimized by centralcomposite design (CCD), then further conjugated with transferrin(Tf) to enhance their GBM targeting ability by targeting the blood-brainbarrier (BBB) and the cancer cells. The obtained NPs exhibited suitableGBM cell delivery features (sizes lower than 200 nm, low polydispersity,and negative surface charge) and a controlled and sustained releasefor 20 days. The uptake and antiproliferative effect of the developedNPs were evaluated in in vitro human GBM models.The obtained results disclosed that the NPs are rapidly taken up bythe GBM cells, promoting synergistic drug effects in inhibiting tumorcell survival and proliferation. This cytotoxicity was associatedwith significant cellular morphological changes. Additionally, thebiocompatibility of unloaded NPs was evaluated in healthy brain cells,demonstrating the safety of the nanocarrier. These findings provethat co-delivery of BTZ and TMZ in Tf-conjugated PLGA NPs is a promisingapproach to treat GBM, overcoming the limitations of current therapeuticstrategies, such as drug resistance and increased side effects.
引用
收藏
页码:14191 / 14203
页数:13
相关论文
共 50 条
  • [31] Synergistic induction of apoptosis in lung cancer cells through co-delivery of PLGA phytol/α-bisabolol nanoparticles
    Kiruthiga, Chandramohan
    Balan, Devasahayam Jaya
    Prasath, Nagaiah Hari
    Manikandakrishnan, Muthushanmugam
    Jafni, Sakthivel
    Prabhu, Narayanasamy Marimuthu
    Pandian, Shunmugiah Karutha
    Devi, Kasi Pandima
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2024, 397 (07) : 5131 - 5144
  • [32] Co-delivery of siRNA and hypericin into cancer cells by hyaluronic acid modified PLGA-PEI nanoparticles
    Li, Yanan
    Zhang, Junling
    Wang, Buhai
    Shen, Yan
    Ouahab, Ammar
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2016, 42 (05) : 737 - 746
  • [33] Transferrin-conjugated, fluorescein-loaded magnetic nanoparticles for targeted delivery across the blood-brain barrier
    Yan, Feng
    Wang, Ying
    He, Shenzhi
    Ku, Shuting
    Gu, Wei
    Ye, Ling
    JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2013, 24 (10) : 2371 - 2379
  • [34] Uptake of transferrin-conjugated quantum dots in single living cells
    Chen, Danni
    Xu, Gaixia
    Ali, Bahi Ahmed
    Yong, Ken-Tye
    Zhou, Cuihong
    Wang, Xiaomei
    Qu, Junle
    Prasad, Paras N.
    Niu, Hanben
    CHINESE OPTICS LETTERS, 2010, 8 (10) : 940 - 943
  • [35] Co-delivery of dexamethasone and melatonin by drugs laden PLGA nanoparticles for the treatment of glaucoma
    Pan, Xue
    Liu, Xuan
    Zhuang, Xianli
    Liu, Yanping
    Li, Shujie
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2020, 60
  • [36] Transferrin-conjugated pH-sensitive platform for effective delivery of porous palladium nanoparticles and paclitaxel in cancer treatment
    Hanh Thuy Nguyen
    Soe, Zar Chi
    Yang, Kwan Yeol
    Cao Dai Phung
    Lan Thi-Trinh Nguyen
    Jeong, Jee-Heon
    Jin, Sung Giu
    Choi, Han-Gon
    Ku, Sae Kwang
    Yong, Chul Soon
    Kim, Jong Oh
    COLLOIDS AND SURFACES B-BIOINTERFACES, 2019, 176 : 265 - 275
  • [37] Transferrin-Conjugated Manganese Dioxide/Semiconducting Polymer Hybrid Nanoparticles for Targeted Dual-Model Imaging of Orthotopic Glioblastoma
    Yu, Ningyue
    Wang, Yue
    Xia, Jindong
    Abashkin, Viktar
    Zhao, Lingzhou
    Li, Jingchao
    ACS APPLIED POLYMER MATERIALS, 2023, 5 (06) : 4596 - 4603
  • [38] Targeted Delivery of Doxorubicin Using Transferrin-Conjugated Carbon Dots for Cancer Therapy
    Li, Lihong
    Zhang, Qi
    Li, Jinyao
    Tian, Yafei
    Kang, Yu
    Ren, Guodong
    Liu, Wen
    Wang, Haojiang
    Wang, Bin
    Yan, Lili
    Guo, Lixia
    Diao, Haipeng
    ACS APPLIED BIO MATERIALS, 2021, 4 (09) : 7280 - 7289
  • [39] Transferrin-conjugated liposomal system for improved delivery of 5-fluorouracil to brain
    Soni, Vandana
    Kohli, D. V.
    Jain, S. K.
    JOURNAL OF DRUG TARGETING, 2008, 16 (01) : 73 - 78
  • [40] Transferrin-Conjugated Pluronic Niosomes as a New Drug Delivery System for Anticancer Therapy
    Tavano, Lorena
    Muzzalupo, Rita
    Mauro, Loredana
    Pellegrino, Michele
    Ando, Sebastiano
    Picci, Nevio
    LANGMUIR, 2013, 29 (41) : 12638 - 12646