Evidence map›Paper›PMID 41880017›Full record

ArticleAnalytical and bioanalytical chemistry2026

Encapsulation efficiency determination methods for the analysis of different antigenic peptides within phosphatidylserine-liposomes.

Irene Latorre, Montserrat Mancera-Arteu, Oumaima El Ouahabi, Míriam Salvadó, Sílvia Rodríguez-Vidal, Victoria Sanz-Nebot

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Article in Analytical and bioanalytical chemistry, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Irene LatorreDepartment of Chemical Engineering and Analytical Chemistry, Institute for Research on Nutrition and Food Safety (INSA·UB), University of Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain.
Montserrat Mancera-ArteuDepartment of Chemical Engineering and Analytical Chemistry, Institute for Research on Nutrition and Food Safety (INSA·UB), University of Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain. montsemancera@ub.edu.
Oumaima El OuahabiDepartment of Chemical Engineering and Analytical Chemistry, Institute for Research on Nutrition and Food Safety (INSA·UB), University of Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain.
Míriam SalvadóAhead Therapeutics SL, Barcelona, Spain.
Sílvia Rodríguez-VidalAhead Therapeutics SL, Barcelona, Spain.
Victoria Sanz-NebotDepartment of Chemical Engineering and Analytical Chemistry, Institute for Research on Nutrition and Food Safety (INSA·UB), University of Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain.

Funding

Agència de Gestió d'Ajuts Universitaris i de Recerca 2022 DI 98Ministerio de Economía y Competitividad RT2018-097411-B-100
6 · The paper itself

Abstract

The prevalence of autoimmune diseases (AIDs) is increasing and persists in individuals of all ages as reported by Pisetsky (Nat Rev Nephrol, 2023). Only palliative treatments are currently available as the development of a treatment that selectively eliminates the immune system autoreaction, without affecting its normal functioning, is not an easy task. In this regard, an innovative strategy based on phosphatidylserine-liposomes (PS-Liposomes) loaded with the autoantigenic peptide that triggers the autoimmune attack has demonstrated efficacy in different AIDs as described by Almenara-Fuentes et al. (Nanomedicine 48, 2023) and Pujol-Autonell et al. (PLoS One 10, 2015). Encapsulation efficiency (EE) determination in liposomal therapeutic formulations is considered one of the most important attributes, as the encapsulated drug concentration is usually related to the treatment's effectiveness. In this regard, several methods have been described in the literature for the determination of specific peptides within liposomes. However, the described methodologies cannot usually be applied to other peptides with different properties. In this study, peptides with different lengths and physicochemical properties encapsulated in PS-Liposome formulations were used as models to evaluate several methods for both free and total antigen quantification. Different approaches for liposome lysis and subsequent total or encapsulated antigen quantification were studied. On the other hand, a comprehensive comparison of different centrifugal filters and an ultracentrifugation method was performed for free antigen determination. Identification and quantification of the autoantigenic peptides were performed by reversed-phase high-performance liquid chromatography with ultraviolet detection (RP-HPLC-UV). Results obtained for direct and indirect EE determinations were compared for PS-Liposome formulations, and the best conditions for each peptide were selected.

Indexed as

AntigensLiposomesPeptidesPhosphatidylserinesChromatography, High Pressure LiquidHumansAntigensLiposomesPeptidesPhosphatidylserinesAutoantigenic peptidesAutoimmune diseasesEncapsulation efficiencyLiquid chromatographyPS-LiposomesUltracentrifugation

Identifiers

PMID41880017
PMCPMC13541897

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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.