Drug, delivery and devices for diabetic retinopathy (3Ds in DR)

Introduction: Diabetic Retinopathy (DR) is one of the most common causes of blindness among the working population worldwide. Clearly, there is an unmet clinical need to find better treatment options for DR. Areas covered: The literature search was conducted on PubMed with no limitation on language...

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Main Authors: Natarajan, Jayaganesh V., Laude, Augustinus, Lim, Tock Han, Venkatraman, Subbu S., Agrawal, Rupesh, Nirmal, Jayabalan, Radhakrishnan, Krishna, Moreno, Miguel
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2016
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Online Access:https://hdl.handle.net/10356/84621
http://hdl.handle.net/10220/41900
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-846212023-07-14T15:57:23Z Drug, delivery and devices for diabetic retinopathy (3Ds in DR) Natarajan, Jayaganesh V. Laude, Augustinus Lim, Tock Han Venkatraman, Subbu S. Agrawal, Rupesh Nirmal, Jayabalan Radhakrishnan, Krishna Moreno, Miguel School of Materials Science & Engineering Diabetic retinopathy Anti-VEGF Introduction: Diabetic Retinopathy (DR) is one of the most common causes of blindness among the working population worldwide. Clearly, there is an unmet clinical need to find better treatment options for DR. Areas covered: The literature search was conducted on PubMed with no limitation on language or year of publication. The review focuses on the clinically used drugs/proteins along with a brief background on the pathophysiology of DR. The major focus of this review revolves around three treatment approaches involving drugs/proteins, drug delivery formulations and drug delivery devices. In each category, major advances are discussed along with the possible solutions. We have also discussed the various modes of administration that are currently being evaluated in the clinic. An attempt has been made to address the potential targeted site of action for DR drug delivery, and also to understand the role of Blood Retinal Barrier (BRB). Expert Opinion: In the current scenario, although there have been some advances in the drug delivery devices for delivering drugs/proteins, there are still challenges to be overcome with regard to the particulate systems. For long-term success of DR therapeutics, research options should consider taking into account the 3Ds (drug, delivery and devices). Accepted version 2016-12-20T09:10:19Z 2019-12-06T15:48:31Z 2016-12-20T09:10:19Z 2019-12-06T15:48:31Z 2016 Journal Article Nirmal, J., Radhakrishnan, K., Moreno, M., Natarajan, J. V., Laude, A., Lim, T. H., et al. (2016). Drug, delivery and devices for diabetic retinopathy (3Ds in DR). Expert Opinion on Drug Delivery, 13(11), 1625-1637. 1742-5247 https://hdl.handle.net/10356/84621 http://hdl.handle.net/10220/41900 10.1080/17425247.2016.1188800 en Expert Opinion on Drug Delivery © 2016 Informa UK Limited. This is the author created version of a work that has been peer reviewed and accepted for publication in Expert Opinion on Drug Delivery, published by Taylor & Francis on behalf of Informa UK Limited. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document.  The published version is available at: [http://dx.doi.org/10.1080/17425247.2016.1188800]. 45 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Diabetic retinopathy
Anti-VEGF
spellingShingle Diabetic retinopathy
Anti-VEGF
Natarajan, Jayaganesh V.
Laude, Augustinus
Lim, Tock Han
Venkatraman, Subbu S.
Agrawal, Rupesh
Nirmal, Jayabalan
Radhakrishnan, Krishna
Moreno, Miguel
Drug, delivery and devices for diabetic retinopathy (3Ds in DR)
description Introduction: Diabetic Retinopathy (DR) is one of the most common causes of blindness among the working population worldwide. Clearly, there is an unmet clinical need to find better treatment options for DR. Areas covered: The literature search was conducted on PubMed with no limitation on language or year of publication. The review focuses on the clinically used drugs/proteins along with a brief background on the pathophysiology of DR. The major focus of this review revolves around three treatment approaches involving drugs/proteins, drug delivery formulations and drug delivery devices. In each category, major advances are discussed along with the possible solutions. We have also discussed the various modes of administration that are currently being evaluated in the clinic. An attempt has been made to address the potential targeted site of action for DR drug delivery, and also to understand the role of Blood Retinal Barrier (BRB). Expert Opinion: In the current scenario, although there have been some advances in the drug delivery devices for delivering drugs/proteins, there are still challenges to be overcome with regard to the particulate systems. For long-term success of DR therapeutics, research options should consider taking into account the 3Ds (drug, delivery and devices).
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Natarajan, Jayaganesh V.
Laude, Augustinus
Lim, Tock Han
Venkatraman, Subbu S.
Agrawal, Rupesh
Nirmal, Jayabalan
Radhakrishnan, Krishna
Moreno, Miguel
format Article
author Natarajan, Jayaganesh V.
Laude, Augustinus
Lim, Tock Han
Venkatraman, Subbu S.
Agrawal, Rupesh
Nirmal, Jayabalan
Radhakrishnan, Krishna
Moreno, Miguel
author_sort Natarajan, Jayaganesh V.
title Drug, delivery and devices for diabetic retinopathy (3Ds in DR)
title_short Drug, delivery and devices for diabetic retinopathy (3Ds in DR)
title_full Drug, delivery and devices for diabetic retinopathy (3Ds in DR)
title_fullStr Drug, delivery and devices for diabetic retinopathy (3Ds in DR)
title_full_unstemmed Drug, delivery and devices for diabetic retinopathy (3Ds in DR)
title_sort drug, delivery and devices for diabetic retinopathy (3ds in dr)
publishDate 2016
url https://hdl.handle.net/10356/84621
http://hdl.handle.net/10220/41900
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