Development of asolectin-based lipid carriers by continuous flow system

Nanoformulation of drugs is a highly important task in medicine to improve their solubility and dissolution. The lipid-based drug delivery systems (LBDDS) facilitate the encapsulation of a broad range of therapeutic agents. Preparation techniques have evolved from simple laboratory "bench" methods to sophisticated, high-throughput technologies. More recently, methods that offer precision, reproducibility, and scalability are in focus as the microfluidics. To the best of our knowledge, we are the first to demonstrate an optimized fabrication protocol of lipid-based colloidal carriers using a low-cost cleaned asolectin (ASO) with a continuously operating basic flow system that offers precise control and high reproducibility. We pointed out how the hydrodynamic diameter, stability, and encapsulation efficiency (EE) can be highly controlled by the initial parameters (flow conditions, pH, storage time, dialysis time, etc.). Tocopherol (TP) and polyvinyl alcohol (PVA) were used as the model drug and stabilizer, respectively. Drug-free carriers having 130 180 nm diameter and 190 300 nm drug-loaded colloids can be fabricated, and it can be confirmed that by nanoformulation the aqueous solubility of TP was increased by 17 20 times. We evaluated the effect of NaCl concentration and pH on the colloids’ stability. The application of the PVA stabilizer slightly increases the EE from 68.6% for ASO/TP to 78.4% for ASO/TP/PVA at a dialysis time of 120 min, and it also enables significant drug retention. In addition to diffusion-controlled processes, the presence of the stabilizer increases the role of carrier erosion, according to the fitting of the dissolution data with different kinetic models. • The flow technique is capable of preparing asolectin-based drug carrier particles. • Size, stability, and formulation ability can be greatly controlled by flow conditions. • Lipid-based nanoformulation of tocopherol increases its water solubility by ∼20 times. • Use of polyvinyl alcohol as a stabilizer enhances the formulation and drug retention.

Authors

Institutions

Publication Details

Journal
Colloids and Surfaces A Physicochemical and Engineering Aspects
Published
2026-03-02
DOI
https://doi.org/10.1016/j.colsurfa.2026.140159
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Development of asolectin-based lipid carriers by continuous flow system

Ádám Juhász, Norbert Varga, Edit Csapó, Egon F. Várkonyi et al.
Colloids and Surfaces A Physicochemical and Engineering Aspects
Lipid Membrane Structure and Behavior
article

Development of asolectin-based lipid carriers by continuous flow system

Ádám Juhász, Norbert Varga, Edit Csapó, Egon F. Várkonyi, L. Serés, Anna Veréb
article en

Abstract

Nanoformulation of drugs is a highly important task in medicine to improve their solubility and dissolution. The lipid-based drug delivery systems (LBDDS) facilitate the encapsulation of a broad range of therapeutic agents. Preparation techniques have evolved from simple laboratory "bench" methods to sophisticated, high-throughput technologies. More recently, methods that offer precision, reproducibility, and scalability are in focus as the microfluidics. To the best of our knowledge, we are the first to demonstrate an optimized fabrication protocol of lipid-based colloidal carriers using a low-cost cleaned asolectin (ASO) with a continuously operating basic flow system that offers precise control and high reproducibility. We pointed out how the hydrodynamic diameter, stability, and encapsulation efficiency (EE) can be highly controlled by the initial parameters (flow conditions, pH, storage time, dialysis time, etc.). Tocopherol (TP) and polyvinyl alcohol (PVA) were used as the model drug and stabilizer, respectively. Drug-free carriers having 130 180 nm diameter and 190 300 nm drug-loaded colloids can be fabricated, and it can be confirmed that by nanoformulation the aqueous solubility of TP was increased by 17 20 times. We evaluated the effect of NaCl concentration and pH on the colloids’ stability. The application of the PVA stabilizer slightly increases the EE from 68.6% for ASO/TP to 78.4% for ASO/TP/PVA at a dialysis time of 120 min, and it also enables significant drug retention. In addition to diffusion-controlled processes, the presence of the stabilizer increases the role of carrier erosion, according to the fitting of the dissolution data with different kinetic models. • The flow technique is capable of preparing asolectin-based drug carrier particles. • Size, stability, and formulation ability can be greatly controlled by flow conditions. • Lipid-based nanoformulation of tocopherol increases its water solubility by ∼20 times. • Use of polyvinyl alcohol as a stabilizer enhances the formulation and drug retention.

Colloids and Surfaces A Physicochemical and Engineering AspectsVol. 739
University of Szeged (HU)
Openalex Percentile: Top 37%
Lipid Membrane Structure and Behavior
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.