Preparation Modification and Characterization of a Hydrogel Based on Polyacrylic and Polymetacrylic Acid as a Potential Carrier for Drug Delivery Systems

Introduction

The excellent biocompatibility and biodegradability of alginate make it very widely used for biomedical application and especially for drug delivery systems and tissue engineering [1, 2]. Different functions and applications of the polymer can be derived due to its possibility for easy chemical modifications. These modifications lead to obtaining of derivatives with various structures and properties [3]. The alginate forms a gel the in presence of different polyvalent metal cations because of the polymer chains cross- linking [4, 5, 6]. Polyectrolyte complexes between sodium alginate and cationic polymers were investigated for the purposes of drug delivery and tissue engineering [7]. For example, films based on sodium alginate and chitosan complexes are proposed for transdermal drug delivery [8, 9, 10]. There are numerous reports of the complexation of polysaccharides with polycarboxylic acidsin aqueous solution [11, 12, 13, 14]. Being a polysaccharide, AL must also form complexes with PAA and PMA. The goal of this work is to study the complexation of AL with PAA and PMA in aqueous media. The formation of interpolyelectrolyte complexes is a significant difference between the properties of such polymer complexes in comparison to the monomers alone. This is a prerequisite for considering such polyelectrolyte complexes as new class polymer compounds [15, 16].

Methods and Materials

Sodium alginate was purchased from Sigma Aldrich, Germany. Acrylic acid was purchased from Sigma Aldrich, Germany. Methacrylic acid was purchased from Sigma Aldrich, Germany. N,Nmethylenebisacrylamide (MBAL) from Sigma Aldrich, Germany. Ammonium persulfate (NH4)2S2O8 was purchased from Sigma Aldrich, Germany. Sodiummetabisulfite Na2S2O5 was purchased from Sigma Aldrich, Germany.

Results and Discussion

Dependences of specific viscosity ηsp of aqueous mixed solution of SAL with PAA and PMA at a constant concentration of a polyacid (PA) on the φ = [SAL]/ [PA], mass/mass ratio, where [SAL] is the mass concentration of SAL and [PA] = const = 0.01 g/dL is shown on the Figure 1.

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Data show that SAL forms complexes with PAA and PMA in aqueous solution. At low concentrations, the system forms true solution without gelation. The incorporation of SAL macromolecules into a solution of a free PA leads to a decrease in solution ηsp. This effect results from the formation of PA-SAL complex particles, which have a more compact conformation than initial PAA or PMA macromolecules have. The compaction of the complex particles is caused by the formation of hydrogen bonds between COOH groups of a PA and COOH groups of SAL. The value of φ that corresponds to the minimum of the ηsp(φ) dependence is in consistence with the composition of a PA/SAL complex. At this value of ϕ, the number of hydrogen bonds between COOH groups of a polyacid and COOH groups of SAL in the complex is far from maximum, because of steric hindrances. The following gradual increase in the viscosity of the system is due to the accumulation of free SAL this is confirmed by the concentration dependence of ηsp for solutions of free SAL.

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The formation of hydrogen bond between SAL, PAA and PMA can be proven also by the IR spectra of the polymers alone and the spectrum of IPC (PAA-SAL and PMA-SAL) [17]. The absorption band at 1711 cm–1, which corresponds to the stretching vibrations νC=O in free PAA, shifts to 1736 cm–1 upon its complexation with SAL. The νC=O band of free PMA visible at 1703 cm–1 shifts to 1717 cm–1 for the complex with SAL. The formation of a chemical (covalent or hydrogen) bond between the functional groups of interacting polymers increases the energy required for the excitation of stretching vibrations in a complexed functional group. Therefore, the stretching vibrations νC=O in PAA, PMA and SAL shift to the region of higher frequencies in our case. Dependences of swelling indices Q of hydrogels based on (1) free SAL and (2) PMA/SAL and (3) PAA/SAL complexes on the pH of an aqueous mediumis shown on Figure 2. The values of Q depend on pH, because SAL, PAA and PMA macromolecules contain weakly acidic groups. Тhe degree of ionization of hydrogels containing pendent carboxyl groups increases at high pH, leading to increased electrostatic repulsions between negatively-charged carboxyl groups, thus resulting in a great swelling degree in response to basic conditions. Absolute value of Q for the hydrogel of the PMA/SAL complex is lower than that for the hydrogel of free SAL. This is due to hydrophobic interactions performed during the complexation between PMA and SAL. The PAA/SAL complex is thermodynamically less stable than the PMA/SAL complex caused by the fact that the presence of CН3 groups in PMA monomer units enhances the hydrophobic interactions upon the complexation with SAL. The PAA/SAL complex swells to a greater extent at comparable value of pH. Hydrogel of the complex between crosslinked PAA and linear SAL remains sensitive to pH, but at the same time, retains its structural integrity. At pH ≈ 8 complex loses its mechanical strength form a dispersion of insoluble particles. The swelling of the hydrogel based on the complex of crosslinked PAA and SAL is of a reversible character. Upon a reduction in pH from 10 to 4 during the back titration of the hydrogel, the dependence of its swelling index Q on pH coincides with curve for the direct titration of the hydrogel. It can be concluded that the hydrogel based on crosslinked PAA and SAL is a pH sensitive structural stable system.

Conclusion

Using IR spectroscopy and viscometry, it has been shown that PAA and PMA form complexes with SAL in aqueous solutions. The complexation is realized via hydrogen bonding between nondissociated COOH groups of the polyacids and COOH groups of the polysaccharides. In the case of SAL-PMA complexation, hydrophobic interactions play an essential role in the stabilization of the complex. The PAA and PMA complexes with SAL represent hydrogels. The hydrogels based on complexes of crosslinked PAA and PMA with SAL represent systems sensitive to pH and can be used as polymeric carriers for pharmaceutically active compounds.