{"title":"Hemoglobin-Polyvinyl Alcohol (Hb-PVA) Macroporous Cryogels As Swelling-Controlled Drug Delivery System Optimization and Release Kinetics of Vancomycin","authors":"Arti Vishwkarma, Jaya Bajpai, A. K. Bajpai","doi":"10.1007/s12247-024-09909-8","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><p>The purpose of this study was to formulate and investigate biopolymer based cryogel as bioactive carriers, which is hydrophilic in nature.</p><h3>Methods</h3><p>A Contemporary research based on the preparation of hemoglobin protein-polyvinyl (Hb-PVA) macroporous cryogels of varying compositions through the freeze–thaw method, using deionized water as a plasticizer. Vancomycin drug loaded Hb-PVA gel applicable as a good platform to promote controlled antibiotic drug release into the specific sites of the body against antibiotic resistance diseases.</p><h3>Results</h3><p>The synthesized Hb-PVA cryogels were characterized by spectroscopic and microscopic techniques such as Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD). Additionally, the morphological and thermal stability of the synthesized cryogels were studied by scanning electron microscopy (SEM) and differential scanning calorimetry. FTIR and XRD spectral assignments revealed the crystalline nature of the cryogel with semicrystalline segments. In addition, scanning electron microscopy (SEM) images revealed that the surface morphology was macroporous in nature; hence, the water-holding capacity of these materials increased. Atomic force microscopy images reveal that the surface roughness is enough for the adhesion of drug molecules, and the R<sub>a</sub>/R<sub>q</sub> ratio is equal to 1.24 for a Gaussian surface. The swelling properties of the prepared cryogels were investigated at different polymer compositions, temperatures, simulated biological solutions, pH media, salt solutions, and freeze thaw cycles at certain time intervals. The swollen gels were further investigated for vancomycin drug loading and release profiles under in vitro conditions, such as changes in the polymer (PVA, Hb) concentration, temperature, and pH of the release media. This drug-loaded cryogel was also examined for its antibacterial activity against gram-positive and gram-negative bacteria.</p><h3>Conclusions</h3><p>The protein based cryogels have great potential to deliver antibiotic drugs or other bioactive compounds. Based ontheir pore-sizes they may also use in water treatment and cell proliferation, wound dressing etc.</p></div>","PeriodicalId":656,"journal":{"name":"Journal of Pharmaceutical Innovation","volume":"20 1","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmaceutical Innovation","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s12247-024-09909-8","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose
The purpose of this study was to formulate and investigate biopolymer based cryogel as bioactive carriers, which is hydrophilic in nature.
Methods
A Contemporary research based on the preparation of hemoglobin protein-polyvinyl (Hb-PVA) macroporous cryogels of varying compositions through the freeze–thaw method, using deionized water as a plasticizer. Vancomycin drug loaded Hb-PVA gel applicable as a good platform to promote controlled antibiotic drug release into the specific sites of the body against antibiotic resistance diseases.
Results
The synthesized Hb-PVA cryogels were characterized by spectroscopic and microscopic techniques such as Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD). Additionally, the morphological and thermal stability of the synthesized cryogels were studied by scanning electron microscopy (SEM) and differential scanning calorimetry. FTIR and XRD spectral assignments revealed the crystalline nature of the cryogel with semicrystalline segments. In addition, scanning electron microscopy (SEM) images revealed that the surface morphology was macroporous in nature; hence, the water-holding capacity of these materials increased. Atomic force microscopy images reveal that the surface roughness is enough for the adhesion of drug molecules, and the Ra/Rq ratio is equal to 1.24 for a Gaussian surface. The swelling properties of the prepared cryogels were investigated at different polymer compositions, temperatures, simulated biological solutions, pH media, salt solutions, and freeze thaw cycles at certain time intervals. The swollen gels were further investigated for vancomycin drug loading and release profiles under in vitro conditions, such as changes in the polymer (PVA, Hb) concentration, temperature, and pH of the release media. This drug-loaded cryogel was also examined for its antibacterial activity against gram-positive and gram-negative bacteria.
Conclusions
The protein based cryogels have great potential to deliver antibiotic drugs or other bioactive compounds. Based ontheir pore-sizes they may also use in water treatment and cell proliferation, wound dressing etc.
期刊介绍:
The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories:
Materials science,
Product design,
Process design, optimization, automation and control,
Facilities; Information management,
Regulatory policy and strategy,
Supply chain developments ,
Education and professional development,
Journal of Pharmaceutical Innovation publishes four issues a year.