| Literature DB >> 35770237 |
Kumaran Subramanian1, Deivasigamani Balaraman2, Kumaravel Kaliyaperumal3, V Devi Rajeswari4, K Balakrishnan5, P Ronald Ross6, Elumalai Perumal7, Pugazhvendan Sampath Renuga8, Mani Panangal9, Y Swarnalatha10, S Velmurugan11.
Abstract
Hydrogel refers to a three-dimensional cross-linked polymeric network made of synthetic or natural polymers that can hold water in its porous structure. The inclusion of hydrophilic groups in the polymer chains, such as amino, carboxyl, and hydroxyl groups, contributes to the hydrogel's water-holding ability. At physiological temperature and pH, these polymeric materials do not dissolve in water, but they do swell significantly in aqueous media. Hydrogel can be manufactured out of almost any water-soluble polymer, and it comes in a variety of chemical compositions and bulk physical properties. Hydrogel can also be made in a variety of ways. Hydrogel comes in a variety of physical shapes, including slabs, microparticles, nanoparticles, coatings, and films. Due to its ease of manufacture and self-application in clinical and fundamental applications, hydrogel has been widely exploited as a drug carrier. Contact lenses, artificial corneas, wound dressing, suture coating, catheters, and electrode sensors are some of the biomedical applications of hydrogels. The pigment color changes were observed from colorless to pale pink followed by dark reddish-pink. Anthocyanin was produced in large quantities and tested using a UV-visible spectrophotometer. At 450-550 nm, the largest peak (absorbance) was detected, indicating the presence of anthocyanin. The FTIR analysis of this study shows the different stretches of bonds at different peaks: 2918.309 (-C-H alkane stretch), 2812.12 (-C-H aldehyde weak intensity), 192320.37/cm (C-O bend), 21915.50, 2029.08/cm (-C=C arene group), 1906.94/cm (=C-H aromatics), 1797.78/cm (=C-H), 1707.94 (-C=O ketene), 1579.70, 1382.96 (C-H alkane strong bend), 889.18/cm (C-H aromatics plane bend), and 412.77/cm (-C-CI strong bond). The spectra of the PVA/chitosan film depict the peak's formation: 1571.88, 1529.55, 1500.62/cm (C-H alkene strong bend), 1492.90, 1483.26, 1467.83/cm (C-H alkene strong bond), 670.48, 443.63, 412.77/cm (-O-H carboxylic acids with great intensity), 1708.93 (-C=O ketone), and 1656.0/cm (alkenyl C=C stretch strong bond).Entities:
Year: 2022 PMID: 35770237 PMCID: PMC9236817 DOI: 10.1155/2022/7975873
Source DB: PubMed Journal: Bioinorg Chem Appl Impact factor: 4.724
Figure 1Sulfuric acid (H2SO4) test.
Figure 2Sodium Hydroxide test of anthocyanin.
Figure 3Color change of anthocyanin from pH 1 (left) to pH 13 (right).
Figure 4Preparation of pH film.
Figure 5FTIR analysis spectrum of PVA/CS/ATH.
Figure 6FTIR analysis spectrum of PVA/CS.
Figure 7Circular dichroism of PVA/CS.
Figure 8The spectra of PVA/Chitosan.
Figure 9SEM image of Sample 1.
Figure 10SEM image of Sample 2.