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      Thermosensitive hexanoyl glycol chitosan-based ocular delivery system for glaucoma therapy.

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          Abstract

          Conventional eye drops quickly move away from the surface of the eye; as a result, ocular bioavailability is very limited. To overcome this issue, we developed a thermosensitive hexanoyl glycol chitosan (HGC) as a carrier for topical drug delivery to the eye. Here, we modulated the degree of N-hexanoylation to control the thermogelling behavior and prepared a new ocular formulation of HGC for glaucoma therapy. The viscosity of the aqueous formulation sharply and significantly increases at body temperature. The results from cytotoxicity evaluation showed that HGC is non-toxic at up to 1.25wt.%. In vivo experiments demonstrated that HGC is maintained on the preocular surface for a comparatively longer period of time due to its enhanced viscosity at body temperature. As a result, when brimonidine was loaded, the formulation exhibited attractive bioavailability properties as well as more prolonged period of lowered intra-ocular pressure (14h) compared with Alphagan P, the marketed medication for brimonidine treatment.

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          Author and article information

          Journal
          Acta Biomater
          Acta biomaterialia
          Elsevier BV
          1878-7568
          1742-7061
          Jul 15 2016
          : 39
          Affiliations
          [1 ] Department of Polymer Science and Engineering, Chungnam National University, Daejeon 305-764, Republic of Korea.
          [2 ] Institute of Medical & Biological Engineering, Medical Research Center, Seoul National University, Seoul 110-799, Republic of Korea.
          [3 ] Interdisciplinary Program in Bioengineering, College of Engineering, Seoul National University, Seoul 152-742, Republic of Korea.
          [4 ] Department of Polymer Science and Engineering, Chungnam National University, Daejeon 305-764, Republic of Korea; Next-generation Pharmaceutical Research Center, Korea Institute of Toxicology, Daejeon 341-114, Republic of Korea.
          [5 ] Department of Polymer Science and Engineering, Chungnam National University, Daejeon 305-764, Republic of Korea; College of Chemical Engineering and Materials Science, Tianjin University of Science & Technology, Tianjin 300-457, China.
          [6 ] Next-generation Pharmaceutical Research Center, Korea Institute of Toxicology, Daejeon 341-114, Republic of Korea; Human and Environmental Toxicology Program, University of Science and Technology, Daejeon 305-350, Republic of Korea.
          [7 ] Institute of Medical & Biological Engineering, Medical Research Center, Seoul National University, Seoul 110-799, Republic of Korea; Interdisciplinary Program in Bioengineering, College of Engineering, Seoul National University, Seoul 152-742, Republic of Korea; Department of Biomedical Engineering, Seoul National University College of Medicine, Seoul 110-799, Republic of Korea. Electronic address: ybchoy@snu.ac.kr.
          [8 ] Department of Polymer Science and Engineering, Chungnam National University, Daejeon 305-764, Republic of Korea. Electronic address: khuh@cnu.ac.kr.
          Article
          S1742-7061(16)30220-3
          10.1016/j.actbio.2016.05.011
          27163401
          8067c865-09ff-4c6e-9070-2cf412782b0d
          History

          Glaucoma therapy,Hexanoyl glycol chitosan,Ocular delivery,Thermosensitive property

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