Background: Drug toxicity and inefficacy are commonly experienced problems with drug therapy failure. To face these problems, extensive research work took place aiming to design new dosage forms for drug delivery especially nanoparticulate systems. These systems are designed to increase the quantity of the therapeutic molecule delivered to the desired site concurrently with reduced side effects. In order to achieve this objective, nanocarriers must principally display suitable drug vehiculization abilities and a controlled biological destiny of drug molecules. Only the intelligent design of the nanomedicine will accomplish these fundamentals. Methods: The present review article is dedicated to the discussion of the important fundamentals to be considered in the fabrication of nanomedicines. These include the therapeutic agent, the imaging agent, the nanocarrier and the functionalization moieties. Special consideration is devoted to the explanation and compilation of highly potential fabrication approaches assisting how to control the in vivo destiny of the nanomedicine. Finally, some nanotechnology-based drug delivery systems, for the development of nanomedicine, are also discussed. Results: The nanotechnology-based drug delivery systems show remarkable outcomes based on passive and active targeting as well as improvement of the drug pharmacodynamic and pharmacokinetic profiles. Multifunctional nanocarrier concept affords a revolutionary drug delivery approach for maximizing the efficacy, safety and monitoring the biological fate of the therapeutic molecule. Conclusion: Nanomedicines may enhance the efficacy of therapeutic molecules and reduce their toxic effects. Meanwhile, further research works are required to rightly optimize (and define) the effectiveness, nanotoxicity, in vivo destiny and feasibility of these nanomedicines which, from a preclinical standpoint, are actually promising.
机构:
City Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
City Univ Hong Kong, Dept Phys & Mat Sci, Hong Kong, Hong Kong, Peoples R ChinaCity Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
Yan, Li
Yang, Yang
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机构:
City Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
City Univ Hong Kong, Dept Phys & Mat Sci, Hong Kong, Hong Kong, Peoples R ChinaCity Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
Yang, Yang
Zhang, Wenjun
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City Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
City Univ Hong Kong, Dept Phys & Mat Sci, Hong Kong, Hong Kong, Peoples R ChinaCity Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
Zhang, Wenjun
Chen, Xianfeng
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City Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
City Univ Hong Kong, Dept Phys & Mat Sci, Hong Kong, Hong Kong, Peoples R ChinaCity Univ Hong Kong, COSDAF, Hong Kong, Hong Kong, Peoples R China
机构:
MIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
Brigham & Womens Hosp, Lab Nanomed & Biomat, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USAMIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
Shi, Jinjun
Votruba, Alexander R.
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Brigham & Womens Hosp, Lab Nanomed & Biomat, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USAMIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
Votruba, Alexander R.
Farokhzad, Omid C.
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机构:
MIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
Brigham & Womens Hosp, Lab Nanomed & Biomat, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USAMIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
Farokhzad, Omid C.
Langer, Robert
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MIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
MIT, Dept Chem Engn, Cambridge, MA 02139 USAMIT, MIT Harvard Ctr Canc Nanotechnol Excellence, Cambridge, MA 02139 USA
机构:
Univ Colorado, Dept Pharmaceut Sci, Aurora, CO USA
Univ Colorado, Dept Ophthalmol, Aurora, CO USA
Univ Colorado, Dept Bioengn, Aurora, CO USAUniv Colorado, Dept Pharmaceut Sci, Aurora, CO USA