Evidence map›Paper›PMID 40462833›Full record

ArticleInternational journal of nanomedicine2025

Development and Optimization of Oral Dissolution Films for Enhanced Delivery of Ebastine-Loaded Solid Lipid Nanoparticles.

Kai Chen, Yong Sun

Abstract read
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Article in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Kai ChenDepartment of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, 266021, People's Republic of China.
Yong SunDepartment of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, 266021, People's Republic of China.ORCID 0000-0003-0365-1151

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Approximately 10-30% of the worldwide population suffers from allergic diseases. Although ebastine (EBT) is described as a potential treatment for allergies, its effects are compromised due to poor solubility and low bioavailability. Methods: This study introduced a novel delivery platform for ebastine by combining solid lipid nanoparticles (SLNs) with oral dissolution films (ODFs). Ebastine SLNs were fabricated using hot melt and ultrasonic emulsification methods, and the SLNs' formulation was optimized by a central composite rotatable design. The developed SLNs were further introduced into a mixed polymer solution of PVA and HPMC to prepare ODFs using the solvent casting method. Results: The optimized EBT-SLNs with spherical structures demonstrated nanoparticle size (147.5 ± 3.32 nm), low polydispersity index (PDI, 0.106 ± 0.005), high entrapment efficiency (86.7%), as well as drug loading (10.02%), respectively. The optimum formulation of ODFs was composed of equal proportion of HPMC and PVA according to normalization methods by evaluation of physicochemical properties including physical appearance, folding endurance and disintegration time. Scanning electron microscopy results disclosed that EBT-SLNs were confined within the network of ODFs and no aggregation SLNs was found. Reconstitution experiments showed EBT-SLNs were still within the nanometers range and maintained a homogenous state, suggesting that incorporation of SLNs into ODFs not compromised their nanoparticulate properties. The in vitro drug release patterns from ODFs containing EBT-SLNs exhibited a fast release profile compared to the commercial EBT tablets. Discussion: The developed system demonstrates enhanced solubility, stability, and bioavailability of ebastine, offering a promising alternative to traditional oral tablets, with potential advantages in patient compliance and rapid drug onset. Therefore, the ODFs containing SLNs can be considered as an efficient approach for EBT administration.

Indexed as

ButyrophenonesLipidsNanoparticlesPiperidinesAdministration, OralBiological AvailabilityDrug CarriersDrug Delivery SystemsDrug LiberationParticle SizePolyvinyl AlcoholSolubilityButyrophenonesDrug CarriersebastineLipidsPiperidinesPolyvinyl Alcoholcentral composite rotatable designebastineoral dissolution filmssolid lipid nanoparticles

Identifiers

PMID40462833
PMCPMC12132053

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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.