Sustained Drug Release from Smart Nanoparticles in Cancer Therapy: A Comprehensive Review

被引:51
作者
Bai, Xue [1 ]
Smith, Zara [1 ]
Wang, Yuheng [1 ]
Butterworth, Sam [1 ]
Tirella, Annalisa [1 ,2 ]
机构
[1] Univ Manchester, Fac Biol Med & Hlth, Sch Hlth Sci, Div Pharm & Optometry, Oxford Rd, Manchester M13 9PT, Lancs, England
[2] Univ Trento, BIOtech Ctr Biomed Technol, Dept Ind Engn, Via Regole 101, I-38123 Trento, Italy
基金
英国工程与自然科学研究理事会;
关键词
cancer nanomedicine; drug delivery systems; sustained drug release; polymeric nanoparticles; liposomes; microfluidics; POLYMER HYBRID NANOPARTICLES; LOADED PLGA NANOPARTICLES; ADVANCED SOLID TUMORS; IN-VITRO RELEASE; CELL LUNG-CANCER; PHASE-I; DELIVERY-SYSTEMS; ANTITUMOR-ACTIVITY; BIODEGRADABLE NANOPARTICLES; ANTICANCER ACTIVITY;
D O I
10.3390/mi13101623
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Although nanomedicine has been highly investigated for cancer treatment over the past decades, only a few nanomedicines are currently approved and in the market; making this field poorly represented in clinical applications. Key research gaps that require optimization to successfully translate the use of nanomedicines have been identified, but not addressed; among these, the lack of control of the release pattern of therapeutics is the most important. To solve these issues with currently used nanomedicines (e.g., burst release, systemic release), different strategies for the design and manufacturing of nanomedicines allowing for better control over the therapeutic release, are currently being investigated. The inclusion of stimuli-responsive properties and prolonged drug release have been identified as effective approaches to include in nanomedicine, and are discussed in this paper. Recently, smart sustained release nanoparticles have been successfully designed to safely and efficiently deliver therapeutics with different kinetic profiles, making them promising for many drug delivery applications and in specific for cancer treatment. In this review, the state-of-the-art of smart sustained release nanoparticles is discussed, focusing on the design strategies and performances of polymeric nanotechnologies. A complete list of nanomedicines currently tested in clinical trials and approved nanomedicines for cancer treatment is presented, critically discussing advantages and limitations with respect to the newly developed nanotechnologies and manufacturing methods. By the presented discussion and the highlight of nanomedicine design criteria and current limitations, this review paper could be of high interest to identify key features for the design of release-controlled nanomedicine for cancer treatment.
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页数:54
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共 343 条
  • [31] Folic Acid-Terminated Poly(2-Diethyl Amino Ethyl Methacrylate) Brush-Gated Magnetic Mesoporous Nanoparticles as a Smart Drug Delivery System
    Beagan, Abeer M.
    Alghamdi, Ahlam A.
    Lahmadi, Shatha S.
    Halwani, Majed A.
    Almeataq, Mohammed S.
    Alhazaa, Abdulaziz N.
    Alotaibi, Khalid M.
    Alswieleh, Abdullah M.
    [J]. POLYMERS, 2021, 13 (01) : 1 - 14
  • [32] Phase I study of MRX34, a liposomal miR-34a mimic, administered twice weekly in patients with advanced solid tumors
    Beg, Muhammad S.
    Brenner, Andrew J.
    Sachdev, Jasgit
    Borad, Mitesh
    Kang, Yoon-Koo
    Stoudemire, Jay
    Smith, Susan
    Bader, Andreas G.
    Kim, Sinil
    Hong, David S.
    [J]. INVESTIGATIONAL NEW DRUGS, 2017, 35 (02) : 180 - 188
  • [33] Nanomedicine review: clinical developments in liposomal applications
    Beltran-Gracia, Esteban
    Lopez-Camacho, Adolfo
    Higuera-Ciapara, Inocencio
    Velazquez-Fernandez, Jesus B.
    Vallejo-Cardona, Alba A.
    [J]. CANCER NANOTECHNOLOGY, 2019, 10 (01)
  • [34] Phase I study of OSI-7904L, a novel liposomal thymidylate synthase inhibitor in patients with refractory solid tumors
    Beutel, G
    Glen, H
    Schöffski, P
    Chick, J
    Gill, S
    Cassidy, J
    Twelves, C
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (15) : 5487 - 5495
  • [35] Binkhathlan Z., 2019, Nanoarchitectonics in Biomedicine, P507
  • [36] Bio-Path Holdings Inc., 2020, PHAS 1B 2A SINGL ARM
  • [37] Phase I and pharmacokinetic (PK) study of MAG-CPT (PNU 166148):: a polymeric derivative of camptothecin (CPT)
    Bissett, D
    Cassidy, J
    de Bono, JS
    Muirhead, F
    Main, M
    Robson, L
    Fraier, D
    Magnè, ML
    Pellizzoni, C
    Porro, MG
    Spinelli, R
    Speed, W
    Twelves, C
    [J]. BRITISH JOURNAL OF CANCER, 2004, 91 (01) : 50 - 55
  • [38] A copper-free click reaction for the synthesis of redox-responsive water-soluble core cross-linked nanoparticles for drug delivery in cancer therapy
    Biswas, Gargi
    Jena, Bikash Chandra
    Sahoo, Satyagopal
    Samanta, Pousati
    Mandal, Mahitosh
    Dhara, Dibakar
    [J]. GREEN CHEMISTRY, 2019, 21 (20) : 5624 - 5638
  • [39] Nanoparticle-Based Medicines: A Review of FDA-Approved Materials and Clinical Trials to Date
    Bobo, Daniel
    Robinson, Kye J.
    Islam, Jiaul
    Thurecht, Kristofer J.
    Corrie, Simon R.
    [J]. PHARMACEUTICAL RESEARCH, 2016, 33 (10) : 2373 - 2387
  • [40] Phase II study of MTX-HSA in combination with Cisplatin as first line treatment in patients with advanced or metastatic transitional cell carcinoma
    Bolling, C.
    Graefe, T.
    Luebbing, C.
    Jankevicius, F.
    Uktveris, S.
    Cesas, A.
    Meyer-Moldenhauer, W. -H.
    Starkmann, H.
    Weigel, M.
    Burk, K.
    Hanauske, A. -R.
    [J]. INVESTIGATIONAL NEW DRUGS, 2006, 24 (06) : 521 - 527