Advances in Dendrimer-Based Anti-Infective Systems: In Vivo Insights and Perspectives
Charlotte Aparici1,2, Kevin Antraygues1,2, Vania Bernardes-Génisson1,2
1Univ Toulouse, CNRS, LCC, Toulouse, France.
Pharmaceutics
|July 28, 2026
Summary
Dendrimers show promise as novel antimicrobial and anti-infective agents, acting intrinsically or as nanocarriers. While preclinical and clinical data exist, further research is needed to standardize studies and clarify structure-activity relationships for clinical efficacy.
Area of Science:
- Nanotechnology
- Medicinal Chemistry
- Infectious Diseases
Background:
- Antimicrobial resistance necessitates novel anti-infective strategies.
- Dendrimers, branched macromolecules, offer unique platforms for antimicrobial applications.
- They can function as direct antimicrobial agents or as nanocarriers for various therapeutic payloads.
Purpose of the Study:
- To review dendrimer-based anti-infective systems with reported in vivo or clinical evaluations.
- To analyze diverse dendritic architectures and their therapeutic potential against infections.
- To identify current limitations and future directions for dendrimer anti-infective research.
Main Methods:
- Literature review of studies reporting in vivo or clinical evaluation of dendrimer-based anti-infective systems.
- Analysis of various dendrimer scaffolds including PAMAM, poly(L-lysine), and others.
- Inclusion of evidence from infected animal models, pharmacokinetic studies, and clinical trials.
Main Results:
- Diverse dendrimer platforms (PAMAM, poly(L-lysine), etc.) have been investigated.
- PAMAM systems show extensive preclinical exploration; astodrimer (poly(L-lysine) dendrimer) is clinically advanced.
- Evidence includes animal models, PK/biodistribution, and clinical trials, but data is heterogeneous.
Conclusions:
- Dendrimers present a versatile and tunable approach for anti-infective development.
- Heterogeneity in study designs (scaffold, formulation, models) limits direct comparisons.
- Future research requires standardized models, safety/biodistribution studies, and clearer structure-activity relationships for clinical translation.
Keywords:
anti-infective therapyantimicrobial resistanceantiviralbacterial vaginosisdendrimerin vivotuberculosiswound infection

