Poly(amidoamine) Salt Form:  Effect on pH-Dependent Membrane Activity and Polymer Conformation in Solution

• Published in: Biomacromolecules Vol. 5; no. 3; pp. 1102 - 1109
• Main Authors: Wan, Ka-Wai, Malgesini, Beatrice, Verpilio, Ilario, Ferruti, Paolo, Griffiths, Peter C, Paul, Alison, Hann, Anthony C, Duncan, Ruth
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 01.05.2004
• Subjects: Applied sciences; Biological and medical sciences; Biological properties; Erythrocyte Membrane - drug effects; Erythrocyte Membrane - ultrastructure; Exact sciences and technology; General pharmacology; Hemolysis - drug effects; Medical sciences; Microscopy, Electron, Scanning; Molecular Conformation; Organic polymers; Pharmaceutical technology. Pharmaceutical industry; Pharmacology. Drug treatments; Physicochemistry of polymers; Polyamines - chemistry; Polyamines - pharmacology; Properties and characterization; Salts; Solutions; Biological properties; Endothelial cell; Rat; Amidoamine copolymer; Cytotoxicity; Amidoamine polymer; pH; Carboxylate polymer; Hemolysis; Polyampholyte; Rodentia; Melanoma; Red blood cell; Experimental study; In vitro; Polyelectrolyte; Vertebrata; Alcohol copolymer; Mammalia; Cell line; Animal; Counter ion; Aqueous solution; Carboxylate copolymer; Comparative study; Conformation
• ISSN: 1525-7797; 1526-4602
• DOI: 10.1021/bm040007z

On exposure to an acidic pH, linear poly(amidoamine)s (PAAs) cause membrane perturbation and consequently have potential as endosomolytic polymers for the intracellular delivery of genes and toxins. Previous studies used PAAs in the hydrochloride form only. The aim of this study was to investigate systematically the effect of the PAA counterion on pH-dependent membrane activity, general cytotoxicity, and PAA solution properties to help guide optimization of PAA structure for further development of PAA−protein conjugates. PAAs (ISA 1, 4, 22, and 23; M w 10 000−50 000 g/mol) were synthesized to provide a library of PAAs having different counterions including the acetate, citrate, hydrochloride, lactate, phosphate, and sulfate salts. pH-Dependent membrane activity was assessed using a rat red blood cell haemolysis assay (conducted at a starting pH of 7.4, 6.5, or 5.5; 1 mg/mL; 1 h), and general cytotoxicity was investigated using a murine melanoma cell line (B16F10) and a human bladder endothelial-like cell line (ECV-304). Whereas poly(ethyleneimine) was haemolytic at the starting pH of 7.4 at 1 h [∼50% haemoglobin (Hb) release], none of the PAA salts were haemolytic at a starting pH of 7.4 or 6.5. Although PAA acetate, citrate, and lactate were also non-haemolytic at the starting pH of 5.5, the sulfate and hydrochloride forms caused significant haemolysis (up to 80% Hb release) and ISA 22 and 23 phosphate were also markedly haemolytic (∼70% Hb release). These counterion-specific differences were also clearly visible using scanning electron microscopy, which was used to visualize the red blood cell morphology. All PAAs were relatively nontoxic (IC50 ≥ 300−5000 μg/mL) compared to poly-l-lysine (IC50 = 2−10 μg/mL), the PAA hydrochloride salts produced the greatest cytotoxicity, and the B16F10 cells were more sensitive than the ECV-304 cells. Small-angle neutron scattering suggested that ISA 23 hydrochloride had a larger hydrodynamic radius (5.1 ± 0.2 nm) than the citrate salt (3.1 ± 0.2 nm). These results provide indirect evidence for the salt- and pH-dependent changes in the conformation of the polymer coil. This study clearly demonstrates the importance of optimization of the counterion form when developing endosomolytic polymers designed to mediate pH-dependent membrane permeabilization.