Nanotechnology as a Platform for the Development of Injectable Parenteral Formulations: A Comprehensive Review of the Know-Hows and State of the Art

被引:37
作者
Boushehri, Maryam A. Shetab [1 ]
Dietrich, Dirk [2 ]
Lamprecht, Alf [1 ,3 ]
机构
[1] Univ Bonn, Fac Pharm, Dept Pharmaceut, D-53121 Bonn, Germany
[2] Univ Clin Bonn, Dept Neurosurg, D-53105 Bonn, Germany
[3] Univ Bourgogne Franche Comte, Inst Pharm, PEPITE EA4267, F-25000 Besancon, France
关键词
nanotechnology; injectable parenteral formulations; solubility enhancement; controlled release; targeting; adjuvancy; immune activation; TARGETED DRUG-DELIVERY; PH-RESPONSIVE NANOPARTICLES; SOLID LIPID NANOPARTICLES; IRON-OXIDE NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; ANTIGEN-PRESENTING CELLS; BLOOD-BRAIN-BARRIER; POLYMER HYBRID NANOPARTICLES; LIGHT-TRIGGERED RELEASE; IN-VIVO EVALUATION;
D O I
10.3390/pharmaceutics12060510
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Within recent decades, the development of nanotechnology has made a significant contribution to the progress of various fields of study, including the domains of medical and pharmaceutical sciences. A substantially transformed arena within the context of the latter is the development and production of various injectable parenteral formulations. Indeed, recent decades have witnessed a rapid growth of the marketed and pipeline nanotechnology-based injectable products, which is a testimony to the remarkability of the aforementioned contribution. Adjunct to the ability of nanomaterials to deliver the incorporated payloads to many different targets of interest, nanotechnology has substantially assisted to the development of many further facets of the art. Such contributions include the enhancement of the drug solubility, development of long-acting locally and systemically injectable formulations, tuning the onset of the drug's release through the endowment of sensitivity to various internal or external stimuli, as well as adjuvancy and immune activation, which is a desirable component for injectable vaccines and immunotherapeutic formulations. The current work seeks to provide a comprehensive review of all the abovementioned contributions, along with the most recent advances made within each domain. Furthermore, recent developments within the domains of passive and active targeting will be briefly debated.
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页码:1 / 53
页数:53
相关论文
共 405 条
[1]   Somatostatin receptors as a new active targeting sites for nanoparticles [J].
Abdellatif, Ahmed A. H. ;
Aldalaen, Sa'ed M. ;
Faisal, Waleed ;
Tawfeek, Hesham M. .
SAUDI PHARMACEUTICAL JOURNAL, 2018, 26 (07) :1051-1059
[2]   Mucin-1 aptamer-armed superparamagnetic iron oxide nanoparticles for targeted delivery of doxorubicin to breast cancer cells [J].
Aghanejad, Ayuob ;
Babamiri, Hiwa ;
Adibkia, Khosro ;
Barar, Jaleh ;
Omidi, Yadollah .
BIOIMPACTS, 2018, 8 (02) :117-127
[3]   Facilitating the translation of nanomedicines to a clinical product: challenges and opportunities [J].
Agrahari, Vibhuti ;
Agrahari, Vivek .
DRUG DISCOVERY TODAY, 2018, 23 (05) :974-991
[4]   Challenges associated and approaches for successful translation of nanomedicines into commercial products [J].
Agrahari, Vivek ;
Hiremath, Praveen .
NANOMEDICINE, 2017, 12 (08) :819-823
[5]  
Ahmed M, 2015, NANOMEDICINE-UK, V10, P2263, DOI [10.2217/NNM.15.58, 10.2217/nnm.15.58]
[6]   Self-assembled hydrogel nanoparticle of cholesterol-bearing pullulan as a carrier of protein drugs: Complexation and stabilization of insulin [J].
Akiyoshi, K ;
Kobayashi, S ;
Shichibe, S ;
Mix, D ;
Baudys, M ;
Kim, SW ;
Sunamoto, J .
JOURNAL OF CONTROLLED RELEASE, 1998, 54 (03) :313-320
[7]   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
[8]   HER-2-Targeted Nanoparticle-Affibody Bioconjugates for Cancer Therapy [J].
Alexis, Frank ;
Basto, Pamela ;
Levy-Nissenbaum, Etgar ;
Radovic-Moreno, Aleksandar F. ;
Zhang, Liangfang ;
Pridgen, Eric ;
Wang, Andrew Z. ;
Marein, Shawn L. ;
Westerhof, Katrina ;
Molnar, Linda K. ;
Farokhzad, Omid C. .
CHEMMEDCHEM, 2008, 3 (12) :1839-1843
[9]   Hydrogel-embeded vesicles, as a novel approach for prolonged release and delivery of liposome, in vitro and in vivo [J].
Alinaghi, A. ;
Rouini, M. R. ;
Daha, F. Johari ;
Moghimi, H. R. .
JOURNAL OF LIPOSOME RESEARCH, 2013, 23 (03) :235-243
[10]  
Allen TM, 1993, DRUG DELIV, V1, P55, DOI DOI 10.3109/10717549309031342