Intravitreal long-term sustained ranibizumab delivery using injectable microgel-embedded hydrogel

Retinal vascular disease is the leading cause of visual impairment. Although intravitreal drug injections are the most suitable approach for addressing retinal disorders, existing clinical treatments necessitate repeated administration, imposing a substantial burden on patients with various intraocu...

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Bibliographic Details
Main Authors: Simin Lee (Author), Jun Young Park (Author), Hye Kyoung Hong (Author), Joo Young Son (Author), Byungwook Kim (Author), Jae Yong Chung (Author), Se Joon Woo (Author), Ki Dong Park (Author)
Format: Book
Published: Elsevier, 2024-10-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Simin Lee  |e author 
700 1 0 |a Jun Young Park  |e author 
700 1 0 |a Hye Kyoung Hong  |e author 
700 1 0 |a Joo Young Son  |e author 
700 1 0 |a Byungwook Kim  |e author 
700 1 0 |a Jae Yong Chung  |e author 
700 1 0 |a Se Joon Woo  |e author 
700 1 0 |a Ki Dong Park  |e author 
245 0 0 |a Intravitreal long-term sustained ranibizumab delivery using injectable microgel-embedded hydrogel 
260 |b Elsevier,   |c 2024-10-01T00:00:00Z. 
500 |a 1818-0876 
500 |a 10.1016/j.ajps.2024.100947 
520 |a Retinal vascular disease is the leading cause of visual impairment. Although intravitreal drug injections are the most suitable approach for addressing retinal disorders, existing clinical treatments necessitate repeated administration, imposing a substantial burden on patients with various intraocular complications. This study introduces an injectable and biodegradable hyaluronan microgel (Hm)-embedded gelatin-poly(ethylene glycol)-tyramine hydrogel (HmGh) designed for sustained intravitreal ranibizumab (RBZ) delivery to reduce patient burden and minimize the side effects associated with frequent injections. Hm exhibited a controlled RBZ loading capacity and release profile. HmGh effectively controlled the initial burst release and overall release profile. Cytocompatibility and cellular drug efficacy were also demonstrated. In an animal study, HmGh maintained RBZ concentrations in the vitreous and retina for >120 d. Pharmacokinetic studies showed that the half-life of RBZ-loaded HmGh in the vitreous and retina was 2.55 and 2.05 times longer than that of RBZ-loaded Hm, respectively, and 9.58 and 38.46 times longer than that of RBZ solution, respectively. Importantly, the initial RBZ elimination from HmGh to the aqueous humor was significantly reduced compared to that from the Hm and RBZ solutions. Intraocular degradation and safety were comprehensively evaluated using fundus imaging and histological analyses. In conclusion, this injectable microgel-embedded hydrogel formulation is a promising prolonged drug delivery system for treating various posterior segment eye diseases. 
546 |a EN 
690 |a Age-related macular degeneration 
690 |a Ranibizumab 
690 |a Microgel-embedded hydrogel 
690 |a Long-term drug delivery 
690 |a Pharmacokinetics 
690 |a Biodegradation 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Asian Journal of Pharmaceutical Sciences, Vol 19, Iss 5, Pp 100947- (2024) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1818087624000643 
787 0 |n https://doaj.org/toc/1818-0876 
856 4 1 |u https://doaj.org/article/8c5990fe16ad4edca5200b410f2bd4b9  |z Connect to this object online.