Nanoparticle-Based Treatment in Glioblastoma

被引:21
作者
Roque, Diogo [1 ,2 ]
Cruz, Nuno [3 ,4 ]
Ferreira, Hugo Alexandre [3 ]
Reis, Catarina Pinto [3 ,4 ]
Matela, Nuno [3 ]
Herculano-Carvalho, Manuel [1 ]
Cascao, Rita [2 ]
Faria, Claudia C. [1 ,2 ,5 ]
机构
[1] Ctr Hosp Univ Lisboa Norte CHULN, Hosp Santa Maria, Dept Neurosurg, P-1649028 Lisbon, Portugal
[2] Univ Lisbon, Fac Med, Inst Med Mol Joao Lobo Antunes, P-1649028 Lisbon, Portugal
[3] Univ Lisbon, Fac Ciencias, Inst Biofis & Engn Biomed, IBEB, P-1749016 Lisbon, Portugal
[4] Univ Lisbon, Res Inst Med, Fac Farm, iMED ULisboa, Av Prof Gama Pinto, P-1649003 Lisbon, Portugal
[5] Univ Lisbon, Fac Med, Clin Univ Neurocirurgia, P-1649028 Lisbon, Portugal
关键词
glioblastoma; nanoparticles; blood-brain barrier; therapy delivery; MESOPOROUS SILICA NANOPARTICLES; POLYMER HYBRID NANOPARTICLES; BLOOD-BRAIN-BARRIER; CARBON NANOTUBES; DELIVERY; TEMOZOLOMIDE; MECHANISM; THERAPY;
D O I
10.3390/jpm13091328
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Glioblastoma (GB) is a malignant glioma associated with a mean overall survival of 12 to 18 months, even with optimal treatment, due to its high relapse rate and treatment resistance. The standardized first-line treatment consists of surgery, which allows for diagnosis and cytoreduction, followed by stereotactic fractionated radiotherapy and chemotherapy. Treatment failure can result from the poor passage of drugs through the blood-brain barrier (BBB). The development of novel and more effective therapeutic approaches is paramount to increasing the life expectancy of GB patients. Nanoparticle-based treatments include epitopes that are designed to interact with specialized transport systems, ultimately allowing the crossing of the BBB, increasing therapeutic efficacy, and reducing systemic toxicity and drug degradation. Polymeric nanoparticles have shown promising results in terms of precisely directing drugs to the brain with minimal systemic side effects. Various methods of drug delivery that pass through the BBB, such as the stereotactic injection of nanoparticles, are being actively tested in vitro and in vivo in animal models. A significant variety of pre-clinical studies with polymeric nanoparticles for the treatment of GB are being conducted, with only a few nanoparticle-based drug delivery systems to date having entered clinical trials. Pre-clinical studies are key to testing the safety and efficacy of these novel anticancer therapies and will hopefully facilitate the testing of the clinical validity of this promising treatment method. Here we review the recent literature concerning the most frequently reported types of nanoparticles for the treatment of GB.
引用
收藏
页数:14
相关论文
共 68 条
[1]   Nanoparticles in Drug Delivery: From History to Therapeutic Applications [J].
Afzal, Obaid ;
Altamimi, Abdulmalik S. A. ;
Nadeem, Muhammad Shahid ;
Alzarea, Sami I. ;
Almalki, Waleed Hassan ;
Tariq, Aqsa ;
Mubeen, Bismillah ;
Murtaza, Bibi Nazia ;
Iftikhar, Saima ;
Riaz, Naeem ;
Kazmi, Imran .
NANOMATERIALS, 2022, 12 (24)
[2]   Advancement in nanogel formulations provides controlled drug release [J].
Ahmed, Shayan ;
Alhareth, Khair ;
Mignet, Nathalie .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2020, 584
[3]   Brain-targeted, drug-loaded solid lipid nanoparticles against glioblastoma cells in culture [J].
Ak, Guliz ;
Unal, Ayse ;
Karakayali, Tugba ;
Ozel, Buket ;
Gunel, Nur Selvi ;
Sanlier, Senay Hamarat .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2021, 206
[4]   Nanoparticles for Targeting Intratumoral Hypoxia: Exploiting a Potential Weakness of Glioblastoma [J].
Aldea, Mihaela ;
Florian, Ioan Alexandru ;
Kacso, Gabriel ;
Craciun, Lucian ;
Boca, Sanda ;
Soritau, Olga ;
Florian, Ioan Stefan .
PHARMACEUTICAL RESEARCH, 2016, 33 (09) :2059-2077
[5]   Systemic Delivery of an Adjuvant CXCR4-CXCL12 Signaling Inhibitor Encapsulated in Synthetic Protein Nanoparticles for Glioma Immunotherapy [J].
Alghamri, Mahmoud S. ;
Banerjee, Kaushik ;
Mujeeb, Anzar A. ;
Mauser, Ava ;
Taher, Ayman ;
Thalla, Rohit ;
McClellan, Brandon L. ;
Varela, Maria L. ;
Stamatovic, Svetlana M. ;
Martinez-Revollar, Gabriela ;
V. Andjelkovic, Anuska ;
V. Gregory, Jason ;
Kadiyala, Padma ;
Calinescu, Alexandra ;
Jimenez, Jennifer A. ;
Apfelbaum, April A. ;
Lawlor, Elizabeth R. ;
Carney, Stephen ;
Comba, Andrea ;
Faisal, Syed Mohd ;
Barissi, Marcus ;
Edwards, Marta B. ;
Appelman, Henry ;
Sun, Yilun ;
Gan, Jingyao ;
Ackermann, Rose ;
Schwendeman, Anna ;
Candolfi, Marianela ;
Olin, Michael R. ;
Lahann, Joerg ;
Lowenstein, Pedro R. ;
Castro, Maria G. .
ACS NANO, 2022, 16 (06) :8729-8750
[6]   Optimization of Tumor Targeting Gold Nanoparticles for Glioblastoma Applications [J].
Allen, Nicholas C. ;
Chauhan, Rajat ;
Bates, Paula J. ;
O'Toole, Martin G. .
NANOMATERIALS, 2022, 12 (21)
[7]   Nano-Therapies for Glioblastoma Treatment [J].
Alphandery, Edouard .
CANCERS, 2020, 12 (01)
[8]   Glioblastoma chemotherapeutic agents used in the clinical setting and in clinical trials: Nanomedicine approaches to improve their efficacy [J].
Aparicio-Blanco, Juan ;
Sanz-Arriazu, Lorena ;
Lorenzoni, Ricardo ;
Blanco-Prieto, Maria J. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2020, 581
[9]   Role of Convective Flow in Carmustine Delivery to a Brain Tumor [J].
Arifin, Davis Yohanes ;
Lee, Kam Yiu Timothy ;
Wang, Chi-Hwa ;
Smith, Kenneth A. .
PHARMACEUTICAL RESEARCH, 2009, 26 (10) :2289-2302
[10]   RNOP-09: Pegylated liposomal doxorubicine and prolonged temozolomide in addition to radiotherapy in newly diagnosed glioblastoma - a phase II study [J].
Beier, Christoph P. ;
Schmid, Christina ;
Gorlia, Thierry ;
Kleinletzenberger, Christine ;
Beier, Dagmar ;
Grauer, Oliver ;
Steinbrecher, Andreas ;
Hirschmann, Birgit ;
Brawanski, Alexander ;
Dietmaier, Christopher ;
Jauch-Worley, Tanja ;
Koelbl, Oliver ;
Pietsch, Torsten ;
Proescholdt, Martin ;
Ruemmele, Petra ;
Muigg, Armin ;
Stockhammer, Guenther ;
Hegi, Monika ;
Bogdahn, Ulrich ;
Hau, Peter .
BMC CANCER, 2009, 9 :308