Aliphatic Poly(Carbonate)s with Acid Responsive Release Mechanisms for Micellar Anti‐Tumor Drug Delivery

Micellar drug delivery systems have emerged as a versatile platform for improving the solubility, stability, and targeted release of chemo(immuno)therapeutics. This review focuses on micellar formulations that combine two key design principles: the inherent biodegradability of aliphatic poly(carbonate)s and the universal acid-responsive trigger mechanism. These systems are particularly attractive for tumor therapy, where the acidic microenvironment can be exploited for controlled drug release. We differentiate between two major classes: (i) systems employing acid-labile linkages for reversible conjugation of pharmaceutically active compounds, and (ii) systems in which micelle disassembly or polymer backbone degradation is governed by acid-responsive functionalities. Both categories are systematically evaluated according to the chemical motifs enabling acid sensitivity, including oximes, imines, hydrazones, boronate ester, acetals, ketals, and tertiary amines, among others. The review highlights recent advances in synthetic strategies, structure-property relationships, and therapeutic performance, emphasizing how these design elements synergistically enhance drug loading, release kinetics, and biocompatibility. Finally, we discuss current challenges and future directions for translating these smart micellar systems into promising tumor-targeted (immuno-)therapeutics.

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Publication Details

Journal
Macromolecular Rapid Communications
Published
2026-03-13
DOI
https://doi.org/10.1002/marc.202500937
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00
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article

Aliphatic Poly(Carbonate)s with Acid Responsive Release Mechanisms for Micellar Anti‐Tumor Drug Delivery

Lutz Nuhn, Adrian V. Hauck
Macromolecular Rapid Communications
Nanoparticle-Based Drug Delivery
article

Aliphatic Poly(Carbonate)s with Acid Responsive Release Mechanisms for Micellar Anti‐Tumor Drug Delivery

Lutz Nuhn, Adrian V. Hauck
article en

Abstract

Micellar drug delivery systems have emerged as a versatile platform for improving the solubility, stability, and targeted release of chemo(immuno)therapeutics. This review focuses on micellar formulations that combine two key design principles: the inherent biodegradability of aliphatic poly(carbonate)s and the universal acid-responsive trigger mechanism. These systems are particularly attractive for tumor therapy, where the acidic microenvironment can be exploited for controlled drug release. We differentiate between two major classes: (i) systems employing acid-labile linkages for reversible conjugation of pharmaceutically active compounds, and (ii) systems in which micelle disassembly or polymer backbone degradation is governed by acid-responsive functionalities. Both categories are systematically evaluated according to the chemical motifs enabling acid sensitivity, including oximes, imines, hydrazones, boronate ester, acetals, ketals, and tertiary amines, among others. The review highlights recent advances in synthetic strategies, structure-property relationships, and therapeutic performance, emphasizing how these design elements synergistically enhance drug loading, release kinetics, and biocompatibility. Finally, we discuss current challenges and future directions for translating these smart micellar systems into promising tumor-targeted (immuno-)therapeutics.

Macromolecular Rapid Communications
University of Würzburg (DE), Bavarian Polymer Institute (DE)
Openalex Percentile: Top 26%
Nanoparticle-Based Drug Delivery
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