Proof-of-concept study of electrospun PLGA membrane in the treatment of limbal stem cell deficiency

Autor: Charanya Ramachandran, Ilida Ortega, Rob McKean, Sheila MacNeil, Sayan Basu, Virender Singh Sangwan, Pallavi Deshpande, Farshid Sefat, Mala Srivastava
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Zdroj: BMJ Open Ophthalmology, Vol 6, Iss 1 (2021)
Druh dokumentu: article
ISSN: 2397-3269
DOI: 10.1136/bmjophth-2021-000762
Popis: Objective The aim of this study was to assess the safety of poly-lactic co-glycolic acid (PLGA) electrospun membranes as carriers for limbal tissue explants for treatment of limbal stem cell deficiency (LSCD).Methods and analysis Approval was obtained for a first in-man study from the Drug Controller General of India. PLGA membranes were applied to the affected eye of five patients after removal of the vascular pannus. Simple limbal epithelial transplantation was performed and limbal explants were secured on the membrane using fibrin glue followed by a bandage contact lens. Patients were followed up for 1 year with ocular exams including slit lamp exam, corneal thickness measurements, intraocular pressure measurements and recording of corneal vascularisation and visual acuity. Systemic examinations included pain grading, clinical laboratory assessment, blood chemistry and urine analysis at baseline, 3 and 6 months after surgery.Results PLGA membranes completely degraded by 8 weeks post-transplantation without any infection or inflammation. In all five patients, the epithelium regenerated by 3 months. In two in five patients, there was a sustained two-line improvement in vision. In one in five patients, the vision improvement was limited due to an underlying stromal scarring. There was recurrence of pannus and LSCD in two in five patients 6 months after surgery which was not attributable to the membrane. The ocular surface remained clear with no epithelial defects in three in five subjects at 12 months.Conclusion PLGA electrospun membranes show promise as carrier for limbal epithelial cells in the treatment of LSCD.
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