Related Experiment Video
Updated: Jun 4, 2026

The Synthesis of RGD-functionalized Hydrogels as a Tool for Therapeutic Applications
Published on: October 7, 2016
Synthesis and characterization of ionic charged water soluble arginine-based poly(ester amide)
Jun Wu1, Martha A Mutschler, Chih-Chang Chu
1Department of Biomedical Engineering, Cornell University, Ithaca, NY 14853-4401, USA.
Biodegradable L-arginine based poly(ester amide)s (Arg-PEAs) are water-soluble, non-toxic polymers. Their properties can be tuned, and they can form photo-crosslinked hydrogels for potential applications.
Area of Science:
- Polymer Chemistry
- Biomaterials Science
- Organic Synthesis
Background:
- Development of novel biodegradable polymers is crucial for advanced applications.
- L-arginine based polymers offer unique properties due to their inherent functionality.
- There is a need for biocompatible cationic polymers for various uses.
Purpose of the Study:
- To synthesize and characterize a family of water-soluble, positively charged L-arginine based poly(ester amide)s (Arg-PEAs).
- To investigate the structure-property relationships of these novel polymers.
- To explore the potential of Arg-PEAs in forming photo-crosslinked hydrogels.
Main Methods:
- Solution polycondensation of L-arginine derived monomers with dicarboxylic acids.
- Chemical characterization of synthesized monomers and polymers using standard techniques.
- Assessment of polymer solubility, cationic properties, and biocompatibility via MTT assay.
- Photo-crosslinking studies with polyethylene glycol diacrylate.
Main Results:
- Successful synthesis of a series of biodegradable Arg-PEAs with good water solubility.
- Demonstrated tunability of hydrophobic and cationic properties by altering polymer backbone.
- All synthesized Arg-PEAs exhibited excellent non-toxicity to cell lines.
- Arg-PEAs with double bond functionality were effectively photo-crosslinked into hybrid hydrogels.
Conclusions:
- L-arginine based poly(ester amide)s represent a promising class of biodegradable, water-soluble, and non-toxic cationic polymers.
- The tunable nature of Arg-PEAs allows for tailored material properties.
- The ability to form photo-crosslinked hydrogels opens avenues for their use in biomedical applications.
More Related Videos
08:55Facile Protocol for the Synthesis of Self-assembling Polyamine-based Peptide Amphiphiles (PPAs) and Related Biomaterials
Published on: June 25, 2018
12:02An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity
Published on: November 2, 2016
Related Concept Videos
Preparation of Amides
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...
Basicity of Heterocyclic Aromatic Amines
Amides to Carboxylic Acids: Hydrolysis
Acid-catalyzed hydrolysis:
Hydrolysis of amides under acidic conditions yields carboxylic acids. Since the reaction occurs slowly, hydrolysis requires the conditions of heat.
The mechanism begins with the protonation of the carbonyl oxygen by the acid catalyst. The protonation makes the amide carbonyl carbon more...
Ion Exchange
Anionic Chain-Growth Polymerization: Overview
Basicity of Aliphatic Amines
To measure the basicity of amines, two conventions are generally used. The first defines Kb as the basicity constant for the deprotonation reaction of water by the amine, as presented in Figure 1. Conventionally, lower Kb indicates higher...