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Updated: Mar 29, 2026

Microfluidic Production of Lysolipid-Containing Temperature-Sensitive Liposomes
Published on: March 3, 2020
Engineering Stability: Cholesterol-Modulated Liposome Response to Physical and Chemical Stressors for Enhanced
Luísa Morato Ribeiro1,2, Cínthia Caetano Bonatto2, Luciano Paulino Silva1,2
1Postgraduate Program in Nanoscience and Nanobiotechnology, University of Brasília, Brasília 70910-900, DF, Brazil.
None:
Background/Objectives: Liposomes are promising carriers for enhancing antibiotic delivery, but their stability under various stress conditions is crucial for clinical applicability. Methods: This study aimed to evaluate the physicochemical and antimicrobial stability of streptomycin-loaded liposomes subjected to mechanical (bath ultrasonication, probe ultrasonication, ultra-turrax homogenization), thermal (freezing, heating), and chemical (H2O2, Triton X-100, sodium dodecyl sulfate-SDS) stressors. Results: Isolated mechanical stresses (probe ultrasonication, ultrasonic bath, and ultra-turrax) did not significantly affect hydrodynamic diameter (DH), polydispersity index (PdI), or Zeta potential (ZP) (p > 0.05). In contrast, combined ultrasound-freezing stress induced marked destabilization, with DH increasing from ~110 nm to 362 nm (Lc0uf) and from 109 nm to 334 nm (Lc1uf), accompanied by PdI increases from ~0.13 to 0.37-0.41 and a ZP shift in Lc1uf from -43.1 mV to -60.1 mV. Thermal exposure at 75 °C and freezing at -30 °C caused no significant changes in DH or PdI, whereas freezing at -80 °C led to severe destabilization, with over fourfold increases in DH and fivefold increases in PdI; the cholesterol-free formulation (Lc0t-80) reached ~664 nm and a PdI of 0.609. Chemical oxidation with 1% H2O2 did not affect DH, PdI, or ZP, while surfactants (1% Triton X-100 and 1% SDS) significantly altered PdI and ZP in a cholesterol-dependent manner. MIC assays showed that formulations stressed by freezing at -80 °C or by combined ultrasound-freezing retained activity against Escherichia coli (MIC = 50 µg/mL), whereas SDS abolished activity. For Staphylococcus aureus, all stressed formulations remained active, and SDS reduced the MIC from 12.5 to 5.625 µg/mL. Conclusions: These findings demonstrate the robustness and stress-specific stabilization of these liposomal formulations, confirming that the antibiotic's activity is preserved, which highlights their potential for therapeutic use.
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