PMID- 27375781 OWN - NLM STAT- MEDLINE DCOM- 20171030 LR - 20240325 IS - 1838-7640 (Electronic) IS - 1838-7640 (Linking) VI - 6 IP - 9 DP - 2016 TI - The Smart Drug Delivery System and Its Clinical Potential. PG - 1306-23 LID - 10.7150/thno.14858 [doi] AB - With the unprecedented progresses of biomedical nanotechnology during the past few decades, conventional drug delivery systems (DDSs) have been involved into smart DDSs with stimuli-responsive characteristics. Benefiting from the response to specific internal or external triggers, those well-defined nanoplatforms can increase the drug targeting efficacy, in the meantime, reduce side effects/toxicities of payloads, which are key factors for improving patient compliance. In academic field, variety of smart DDSs have been abundantly demonstrated for various intriguing systems, such as stimuli-responsive polymeric nanoparticles, liposomes, metals/metal oxides, and exosomes. However, these nanoplatforms are lack of standardized manufacturing method, toxicity assessment experience, and clear relevance between the pre-clinical and clinical studies, resulting in the huge difficulties to obtain regulatory and ethics approval. Therefore, such relatively complex stimulus-sensitive nano-DDSs are not currently approved for clinical use. In this review, we highlight the recent advances of smart nanoplatforms for targeting drug delivery. Furthermore, the clinical translation obstacles faced by these smart nanoplatforms have been reviewed and discussed. We also present the future directions and perspectives of stimuli-sensitive DDS in clinical applications. FAU - Liu, Dong AU - Liu D AD - State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biomedical Sciences and Medical Engineering, Southeast University, Nanjing, 210009, China. FAU - Yang, Fang AU - Yang F AD - State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biomedical Sciences and Medical Engineering, Southeast University, Nanjing, 210009, China. FAU - Xiong, Fei AU - Xiong F AD - State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biomedical Sciences and Medical Engineering, Southeast University, Nanjing, 210009, China. FAU - Gu, Ning AU - Gu N AD - State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biomedical Sciences and Medical Engineering, Southeast University, Nanjing, 210009, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20160607 PL - Australia TA - Theranostics JT - Theranostics JID - 101552395 SB - IM MH - Animals MH - *Drug Delivery Systems MH - Drug Discovery/*methods/*trends MH - Humans MH - Molecular Targeted Therapy/*methods MH - Nanoparticles/*administration & dosage MH - Theranostic Nanomedicine/*methods PMC - PMC4924501 OTO - NOTNLM OT - Biomaterials OT - Controlled release OT - Drug delivery system (DDS) OT - Nanomedicine. OT - Smart nanoplatform COIS- Competing Interests: The authors have declared that no competing interest exists. EDAT- 2016/07/05 06:00 MHDA- 2017/10/31 06:00 PMCR- 2016/01/01 CRDT- 2016/07/05 06:00 PHST- 2015/12/31 00:00 [received] PHST- 2016/05/22 00:00 [accepted] PHST- 2016/07/05 06:00 [entrez] PHST- 2016/07/05 06:00 [pubmed] PHST- 2017/10/31 06:00 [medline] PHST- 2016/01/01 00:00 [pmc-release] AID - thnov06p1306 [pii] AID - 10.7150/thno.14858 [doi] PST - epublish SO - Theranostics. 2016 Jun 7;6(9):1306-23. doi: 10.7150/thno.14858. eCollection 2016.