Delayed nucleation in lipid particles

TL;DR

This study investigates the delayed crystallization in lipid particles, demonstrating controllable metastable states and deviations from classical nucleation theory, with implications for drug delivery systems.

Contribution

The paper shows how the metastable liquid-crystalline phase of DLPE can be controlled and manipulated, revealing deviations from classical nucleation theory in lipid systems.

Findings

Crystallization delay is a bulk, tunable phenomenon.

Delay can be adjusted over two orders of magnitude by environmental factors.

Metastability persists robustly, resisting classical nucleation predictions.

Abstract

Metastable states in first-order phase-transitions have been traditionally described by classical nucleation theory (CNT). However, recently an increasing number of systems displaying such a transition have not been successfully modelled by CNT. The delayed crystallization of phospholipids upon super-cooling is an interesting case, since the extended timescales allow access into the dynamics. Herein, we demonstrate the controllable behavior of the long-lived metastable liquid-crystalline phase of dilauroyl-phosphatidylethanolamine (DLPE), arranged in multi-lamellar vesicles, and the ensuing cooperative transition to the crystalline state. Experimentally, we find that the delay in crystallization is a bulk phenomenon, which is tunable and can be manipulated to span two orders of magnitude in time by changing the quenching temperature, solution salinity, or adding a secondary phospholipid. Our results reveal the robust persistence of the metastability, and showcase the apparent deviation from CNT. This distinctive suppression of the transition may be explained by the resistance of the multi-lamellar vesicle to deformations caused by nucleated crystalline domains. Since phospholipids are used as a platform for drug-delivery, a programmable design of cargo hold and release can be of great benefit.