Peptide-mediated drug delivery across the blood-brain barrier for targeting brain tumors

被引:52
作者
Jafari, Behzad [1 ,2 ]
Pourseif, Mohammad M. [1 ]
Barar, Jaleh [1 ,3 ]
Rafi, Mohammad A. [4 ]
Omidi, Yadollah [1 ,3 ]
机构
[1] Tabriz Univ Med Sci, Biomed Inst, Res Ctr Pharmaceut Nanotechnol, Tabriz, Iran
[2] Urmia Univ Med Sci, Dept Med Chem, Fac Pharm, Orumiyeh, Iran
[3] Tabriz Univ Med Sci, Dept Pharmaceut, Fac Pharm, Tabriz, Iran
[4] Thomas Jefferson Univ, Coll Med, Dept Neurol, Philadelphia, PA 19107 USA
关键词
Blood-brain barrier; brain drug delivery; brain drug targeting; peptide-drug conjugates; phage display; shuttle peptides; CENTRAL-NERVOUS-SYSTEM; NICOTINIC ACETYLCHOLINE-RECEPTORS; PHAGE-DISPLAY; INTERCELLULAR-JUNCTIONS; INTRACELLULAR DELIVERY; EXTRACELLULAR-MATRIX; ABC-TRANSPORTERS; CYTOTOXIC DRUG; MOUSE MODEL; CANCER;
D O I
10.1080/17425247.2019.1614911
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Transportation of the nutrients and other substances from the blood to the brain is selectively controlled by the brain capillary endothelial cells that form a restrictive barrier, so-called blood-brain barrier (BBB). Currently, there is no unimpeachable approach to overcome the BBB obstructiveness because the existing options are either invasive or ineffective. Areas covered: This review delineates the biological impacts of BBB on brain drug delivery and targeting. The nanoscaled multifunctional shuttles armed with the targeting entities (e.g., antibodies and peptides) are discussed. Important insights are remarked into the combinatorial screening methodologies used for the identification of de novo peptides capable of crossing BBB and targeting the brain. Expert opinion: Depending on the physicochemical properties of small molecules and macromolecules, they may cross the BBB and get into the brain either through passive diffusion or active/facilitated transportation and transcytosis in a very selectively controlled manner. Phage-derived shuttle peptides can specifically be selected against BBB endocytic machinery and used in engineering novel peptide-drug conjugates (PDCs). Nanoscaled multitargeting delivery systems encompassing PDCs can overcome the BBB obstructiveness and deliver drugs specifically to diseased cells in the brain with trivial side effects.
引用
收藏
页码:583 / 605
页数:23
相关论文
共 166 条
[91]   The 2007 WHO classification of tumours of the central nervous system (vol 114, pg 97, 2007) [J].
Louis, David N. ;
Ohgaki, Hiroko ;
Wiestler, Otmar D. ;
Cavenee, Webster K. ;
Burger, Peter C. ;
Jouvet, Anne ;
Scheithauer, Bernd W. ;
Kleihues, Paul .
ACTA NEUROPATHOLOGICA, 2007, 114 (05) :547-547
[92]   Linkers Having a Crucial Role in Antibody-Drug Conjugates [J].
Lu, Jun ;
Jiang, Feng ;
Lu, Aiping ;
Zhang, Ge .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (04)
[93]   Tight junctions at the blood brain barrier: Physiological architecture and disease-associated dysregulation [J].
Anny-Claude Luissint ;
Cédric Artus ;
Fabienne Glacial ;
Kayathiri Ganeshamoorthy ;
Pierre-Olivier Couraud .
Fluids and Barriers of the CNS, 9 (1)
[94]   Peptide-Drug Conjugate: A Novel Drug Design Approach [J].
Ma, Liang ;
Wang, Chao ;
He, Zihao ;
Cheng, Biao ;
Zheng, Ling ;
Huang, Kun .
CURRENT MEDICINAL CHEMISTRY, 2017, 24 (31) :3373-3396
[95]   Astrocytes Maintain Glutamate Homeostasis in the CNS by Controlling the Balance between Glutamate Uptake and Release [J].
Mahmoud, Shaimaa ;
Gharagozloo, Marjan ;
Simard, Camille ;
Gris, Denis .
CELLS, 2019, 8 (02)
[96]   Peptide-mediated targeted drug delivery [J].
Majumdar, Sumit ;
Siahaan, Teruna J. .
MEDICINAL RESEARCH REVIEWS, 2012, 32 (03) :637-658
[97]   Chemical Optimization of New Ligands of the Low-Density Lipoprotein Receptor as Potential Vectors for Central Nervous System Targeting [J].
Malcor, Jean-Daniel ;
Payrot, Nadine ;
David, Marion ;
Faucon, Aude ;
Abouzid, Karima ;
Jacquot, Guillaume ;
Floquet, Nicolas ;
Debarbieux, Franck ;
Rougon, Genevieve ;
Martinez, Jean ;
Khrestchatisky, Michel ;
Vlieghe, Patrick ;
Lisowski, Vincent .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (05) :2227-2241
[98]   Junctional adhesion molecule, a novel member of the immunoglobulin superfamily that distributes at intercellular junctions and modulates monocyte transmigration [J].
Martìn-Padura, I ;
Lostaglio, S ;
Schneemann, M ;
Williams, L ;
Romano, M ;
Fruscella, P ;
Panzeri, C ;
Stoppacciaro, A ;
Ruco, L ;
Villa, A ;
Simmons, D ;
Dejana, E .
JOURNAL OF CELL BIOLOGY, 1998, 142 (01) :117-127
[99]   Regulation of synaptic transmission and plasticity by neuronal nicotinic acetylcholine receptors [J].
McKay, Bruce E. ;
Placzek, Andon N. ;
Dani, John A. .
BIOCHEMICAL PHARMACOLOGY, 2007, 74 (08) :1120-1133
[100]   Regulation of ABC Transporters at the Blood-Brain Barrier [J].
Miller, D. S. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2015, 97 (04) :395-403