Literature DB >> 23298616

Polymeric "smart" coatings to prevent foreign body response to implantable biosensors.

Yan Wang1, Fotios Papadimitrakopoulos, Diane J Burgess.   

Abstract

Application of implantable glucose biosensors for "real-time" monitoring is reliant on controlling the negative tissue reaction at the sensor tissue interphase. A novel polymer coating consisting of poly(lactic-co-glycolic) acid (PLGA) microsphere dispersed in poly(vinyl alcohol) (PVA) hydrogels was evaluated in combination with dummy sensors as a "smart" drug eluting biocompatible coating for implantable biosensors to prevent the foreign body response, and thus enhance sensor performance in vivo. The polymeric microspheres slowly release tissue-modifying drugs at the implantation sites to control the inflammation and fibrous encapsulation, while the hydrogel allows rapid analyte diffusion to the sensing elements. Dummy sensors with identical dimensions to that of the functional glucose sensors (0.5×0.5×5mm) were coated with the PLGA/PVA composites using a mold fabrication process. Both normal and diabetic rats were used in the current study to investigate the effect of the diabetic state on tissue sensor interactions. It was evident that the PLGA/PVA hydrogel composite was able to form a uniform coating around the dummy sensor and stayed intact throughout the course of the study (one month). Tissue samples containing dummy sensors that were coated with dexamethasone free composites exhibited acute and chronic inflammation as well as fibrous encapsulation in both normal and diabetic rats. However, the diabetic rats exhibited decreased intensity and delayed onset of the foreign body response following implantation of drug free dummy sensors in comparison to those of normal rats. On the other hand, tissues containing dummy sensors that were coated with dexamethasone containing composites remained normal (i.e. similar to untreated tissues), with no inflammatory reaction or fibrous encapsulation occurring over the one-month period in both the normal and diabetic rats. The feasibility of utilizing PLGA microsphere/PVA hydrogel composites as coatings for implantable biosensors was demonstrated. This polymeric composite is an innovative approach to control the foreign body reaction at the tissue-device interface to prolong biosensor lifetime.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23298616     DOI: 10.1016/j.jconrel.2012.12.028

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  23 in total

1.  Microspheres prepared with PLGA blends for delivery of dexamethasone for implantable medical devices.

Authors:  Yan Wang; Bing Gu; Diane J Burgess
Journal:  Pharm Res       Date:  2013-08-15       Impact factor: 4.200

2.  Histological evaluation of a chronically-implanted electrocorticographic electrode grid in a non-human primate.

Authors:  Alan D Degenhart; James Eles; Richard Dum; Jessica L Mischel; Ivan Smalianchuk; Bridget Endler; Robin C Ashmore; Elizabeth C Tyler-Kabara; Nicholas G Hatsopoulos; Wei Wang; Aaron P Batista; X Tracy Cui
Journal:  J Neural Eng       Date:  2016-06-28       Impact factor: 5.379

Review 3.  Composites of Polymer Hydrogels and Nanoparticulate Systems for Biomedical and Pharmaceutical Applications.

Authors:  Fuli Zhao; Dan Yao; Ruiwei Guo; Liandong Deng; Anjie Dong; Jianhua Zhang
Journal:  Nanomaterials (Basel)       Date:  2015-12-03       Impact factor: 5.076

4.  PLGA microsphere/PVA hydrogel coatings suppress the foreign body reaction for 6 months.

Authors:  Bing Gu; Fotios Papadimitrakopoulos; Diane J Burgess
Journal:  J Control Release       Date:  2018-09-24       Impact factor: 9.776

5.  Crosslinked basement membrane-based coatings enhance glucose sensor function and continuous glucose monitoring in vivo.

Authors:  Ulrike Klueh; Izabela Ludzinska; Caroline Czajkowski; Yi Qiao; Donald L Kreutzer
Journal:  J Biomed Mater Res A       Date:  2017-09-19       Impact factor: 4.396

6.  Seeing is believing, PLGA microsphere degradation revealed in PLGA microsphere/PVA hydrogel composites.

Authors:  Bing Gu; Xuanhao Sun; Fotios Papadimitrakopoulos; Diane J Burgess
Journal:  J Control Release       Date:  2016-03-08       Impact factor: 9.776

7.  Nanoparticle delivery of miR-223 to attenuate macrophage fusion.

Authors:  Laura Beth Moore; Andrew J Sawyer; Jennifer Saucier-Sawyer; W Mark Saltzman; Themis R Kyriakides
Journal:  Biomaterials       Date:  2016-02-26       Impact factor: 12.479

8.  Localized delivery of dexamethasone-21-phosphate via microdialysis implants in rat induces M(GC) macrophage polarization and alters CCL2 concentrations.

Authors:  Geoffrey D Keeler; Jeannine M Durdik; Julie A Stenken
Journal:  Acta Biomater       Date:  2014-10-25       Impact factor: 8.947

Review 9.  Improving long-term subcutaneous drug delivery by regulating material-bioenvironment interaction.

Authors:  Wei Chen; Bryant C Yung; Zhiyong Qian; Xiaoyuan Chen
Journal:  Adv Drug Deliv Rev       Date:  2018-01-31       Impact factor: 15.470

10.  Prediction of dexamethasone release from PLGA microspheres prepared with polymer blends using a design of experiment approach.

Authors:  Bing Gu; Diane J Burgess
Journal:  Int J Pharm       Date:  2015-09-15       Impact factor: 5.875

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