Evidence map›Paper›PMID 38684590›Full record

ArticleAAPS PharmSciTech2024

Silk Fibroin Formed Bioadhesive Ophthalmic Gel for Dry Eye Syndrome Treatment.

Tianjiao Hao, Lu Tang, Qianzi Xu, Wei Wang, Zengjing Li, Yan Shen, Bohui Xu, Hao Luo, Qian Li, Jirong Wang and 1 more

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Article in AAPS PharmSciTech, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Tianjiao Hao *Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, China.ORCID http://orcid.org/0009-0001-2557-8007
Lu Tang *Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Qianzi Xu *Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Wei WangDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Zengjing LiDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Yan ShenDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Bohui XuSchool of Pharmacy, Nantong University, No.19 Qixiu Road, Nantong, 226001, China.
Hao LuoDepartment of Internal Medicine Oncology, Lianshui People's Hospital, No.6 Hongri East Road, Lianshui, 223400, Jiangsu Province, China.
Qian LiCollage of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
Jirong WangDepartment of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, China. 1481604508@qq.com.
Jinling ZhangJiangsu Institute for Food and Drug Control, Jiangsu Province, Nanjing, China. zjluser@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDry eye syndrome (DES), arising from various etiologic factors, leads to tear film instability and ocular surface damage. Given its anti-inflammatory effects, cyclosporine A (CsA) has been widely used as a short-term treatment option for DES. However, poor bioavailability and solubility of CsA in aqueous phase make the development of a cyclosporine A-based eye drop for ocular topical application a huge challenge.

methodsIn this study, a novel strategy for preparing cyclosporine A-loaded silk fibroin nanoemulsion gel (CsA NBGs) was proposed to address these barriers. Additionally, the rheological properties, ocular irritation potential, tear elimination kinetics, and pharmacodynamics based on a rabbit dry eye model were investigated for the prepared CsA NBGs. Furthermore, the transcorneal mechanism across the ocular barrier was also investigated.

resultsThe pharmacodynamics and pharmacokinetics of CsA NBGs exhibited superior performance compared to cyclosporine eye drops, leading to a significant enhancement in the bioavailability of CsA NBGs. Furthermore, our investigation into the transcorneal mechanism of CsA NBGs revealed their ability to be absorbed by corneal epithelial cells via the paracellular pathway.

conclusionThe CsA NBG formulation exhibits promising potential for intraocular drug delivery, enabling safe, effective, and controlled administration of hydrophobic drugs into the eye. Moreover, it enhances drug retention within the ocular tissues and improves systemic bioavailability, thereby demonstrating significant clinical translational prospects.

Indexed as

Biological AvailabilityCyclosporineDry Eye SyndromesFibroinsGelsOphthalmic SolutionsAdministration, OphthalmicAnimalsCorneaDisease Models, AnimalDrug Delivery SystemsEmulsionsMaleRabbitsSolubilityCyclosporineEmulsionsFibroinsGelsOphthalmic Solutionscyclosporine adry eye syndromeeye irritationophthalmic nanoemulsion with silk fibroin geltranscorneal mechanism

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.