Fabrication and characterization of smart karaya gum/sodium alginate semi-IPN microbeads for controlled release of D-penicillamine drug

This article reports the fabrication of pH-sensitive microbeads from sodium alginate (SA) and modified karaya gum (KG). KG was modified by graft copolymerization using 2-hydroxyethyl methacrylate (2-HEMA) through in situ free radical polymerization reaction. The graft copolymer was blended with SA to develop microbeads by a simple ionotropic gelation technique. The microbeads were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, and scanning electron microscopy. The effect of %HEMA and polymer blend ratio on the swelling capacity was investigated. Drug release kinetics of the microbeads was investigated under both pH 7.4 and pH 1.2 at 37°C. The drug release kinetics was analyzed by evaluating the release data using different kinetic models.

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Synthesis and Characterization of SA-g-MAA Co-Polymer: Effect of Grafting and Process Variables on Controlled Release of an Anti-Bacterial Drug

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.123-125.387 ◽

2010 ◽

Vol 123-125 ◽

pp. 387-390 ◽

Cited By ~ 2

Author(s):

C.V. Prasad ◽

K.M. Sudhan Rao ◽

B. Mallikarjuna ◽

M.C.S. Subha ◽

K. Chowdoji Rao

Keyword(s):

Sodium Alginate ◽

Entrapment Efficiency ◽

Alginate Beads ◽

X Ray Diffraction ◽

Scanning Calorimetry ◽

Potassium Persulphate ◽

Preparation Conditions ◽

Swelling Capacity ◽

Release Profiles

Methacrylic acid (MAA) was grafted onto sodium alginate (SA) by thermal heating at ambient temperature (70±2OC) using potassium persulphate as an initiator (PPS). SA-g-MAA and pure sodium alginate beads were prepared and were characterized using Scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and X-ray diffraction techniques (X-Rd). The resultant products (SA-g-MAA) were used to prepare Glutaraldehyde (GA) crosslinked beads of various formulations by varying, monomer, cross-linker (GA) and drug content (CFHCl) in the graft co-polymer. Preparation conditions of the beads were optimized by considering the percentage entrapment efficiency, swelling capacity and release profiles. Release profile of CFHCl was discussed at 370C in a gastrointestinal atmosphere (pH -7.4 and acidic medium pH-1.2). It was observed that, CFHCl release from the beads increased with increasing MAA content over the entire studied range. As GA and CFHCl content increases, swelling ratio decreases resulting in decrease in the drug release rate. The highest CFHCl release was obtained to be 99% for the beads containing 40% monomer, 0.5mL GA and 10% CFHCl at pH-7.4. It was also observed that the release profiles have effect on pH and hence the graft co-polymeric beads can be used as pH sensitive drug devices.

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Preparation and Characterization of Compounds Based on Poly(hydroxymethylacrylamide) and Post-consumer Polypropylene

Chemistry & Chemical Technology ◽

10.23939/chcht10.03.291 ◽

2016 ◽

Vol 10 (3) ◽

pp. 291-298 ◽

Cited By ~ 1

Author(s):

Ilma Cirne ◽

◽

Maria Esperidiao ◽

Jaime Boaventura ◽

Elizabete Lucas ◽

...

Keyword(s):

Polymer Composites ◽

Food Packaging ◽

Low Cost ◽

Condensation Reaction ◽

Polymerization Reaction ◽

X Ray Diffraction ◽

Scanning Calorimetry ◽

Swelling Capacity ◽

Ft Ir

In this work, in order to obtain materials with potential for treatment of water from oil industry, polymer composites were synthesized by polymerization reaction via free radical using n-hydroxymethyl acrylamide (HMAA) in the presence of post-consumer polypropylene (PP) with subsequent condensation reaction catalyzed by heating, which avoids the use of crosslinking agents. The products were characterized by Fourier transform infrared spectroscopy (FT-IR), optical microscopy (OM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and X-ray diffraction (XRD). Moreover, the bulk density and the degree of swelling were also determined. The synthesis was shown to be reproducible and led to achieving polymer composites with high levels of PP after usage from food packaging, which can be associated with a relatively low cost of production. The swelling capacity and the thermal stability of the composite increased with increasing PP content in the mixture.

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Novel Hydrogels of Chitosan and Poly (vinyl alcohol) Reinforced with Inorganic Particles of Bioactive Glass

Polymers ◽

10.3390/polym13050691 ◽

2021 ◽

Vol 13 (5) ◽

pp. 691

Author(s):

O. Sánchez-Aguinagalde ◽

Ainhoa Lejardi ◽

Emilio Meaurio ◽

Rebeca Hernández ◽

Carmen Mijangos ◽

...

Keyword(s):

Mechanical Properties ◽

Drug Release ◽

Bioactive Glass ◽

Vinyl Alcohol ◽

Release Kinetics ◽

The Body ◽

Poly Vinyl Alcohol ◽

X Ray Diffraction ◽

Inorganic Particles ◽

Release Studies

Chitosan (CS) and poly (vinyl alcohol) (PVA) hydrogels, a polymeric system that shows a broad potential in biomedical applications, were developed. Despite the advantages they present, their mechanical properties are insufficient to support the loads that appear on the body. Thus, it was proposed to reinforce these gels with inorganic glass particles (BG) in order to improve mechanical properties and bioactivity and to see how this reinforcement affects levofloxacin drug release kinetics. Scanning electron microscopy (SEM), X-ray diffraction (XRD), swelling tests, rheology and drug release studies characterized the resulting hydrogels. The experimental results verified the bioactivity of these gels, showed an improvement of the mechanical properties and proved that the added bioactive glass does affect the release kinetics.

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Formulation and development of metformin-loaded microspheres using Khaya senegalensis (Meliaceae) gum as co-polymer

Future Journal of Pharmaceutical Sciences ◽

10.1186/s43094-020-00139-6 ◽

2020 ◽

Vol 6 (1) ◽

Author(s):

Chukwuebuka H. Ozoude ◽

Chukwuemeka P. Azubuike ◽

Modupe O. Ologunagba ◽

Sejoro S. Tonuewa ◽

Cecilia I. Igwilo

Keyword(s):

Controlled Release ◽

Sodium Alginate ◽

Release Kinetics ◽

Drug Carrier ◽

In Vitro Release ◽

Entrapment Efficiency ◽

Metformin Hydrochloride ◽

Scanning Calorimetry ◽

Khaya Senegalensis

Abstract Background Khaya gum is a bark exudate from Khaya senegalensis (Maliaecae) that has drug carrier potential. This study aimed to formulate and comparatively evaluate metformin-loaded microspheres using blends of khaya gum and sodium alginate. Khaya gum was extracted and subjected to preformulation studies using established protocols while three formulations (FA; FB and FC) of metformin (1% w/v)-loaded microspheres were prepared by the ionic gelation method using 5% zinc chloride solution as the cross-linker. The formulations contained 2% w/v blends of khaya gum and sodium alginate in the ratios of 2:3, 9:11, and 1:1, respectively. The microspheres were evaluated by scanning electron microscopy, Fourier transform-infrared spectroscopy, differential scanning calorimetry, entrapment efficiency, swelling index, and in vitro release studies. Results Yield of 28.48%, pH of 4.00 ± 0.05, moisture content (14.59% ± 0.50), and fair flow properties (Carr’s index 23.68 ± 1.91 and Hausner’s ratio 1.31 ± 0.03) of the khaya gum were obtained. FTIR analyses showed no significant interaction between pure metformin hydrochloride with excipients. Discrete spherical microspheres with sizes ranging from 1200 to 1420 μm were obtained. Drug entrapment efficiency of the microspheres ranged from 65.6 to 81.5%. The release of the drug from microspheres was sustained for the 9 h of the study as the cumulative release was 62% (FA), 73% (FB), and 80% (FC). The release kinetics followed Korsmeyer-Peppas model with super case-II transport mechanism. Conclusion Blends of Khaya senegalensis gum and sodium alginate are promising polymer combination for the preparation of controlled-release formulations. The blend of the khaya gum and sodium alginate produced microspheres with controlled release properties. However, the formulation containing 2:3 ratio of khaya gum and sodium alginate respectively produced microspheres with comparable controlled release profiles to the commercial brand metformin tablet.

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Improved antimicrobial property and controlled drug release kinetics of silver sulfadiazine loaded ordered mesoporous silica

Journal of Asian Ceramic Societies ◽

10.1016/j.jascer.2016.05.005 ◽

2016 ◽

Vol 4 (3) ◽

pp. 282-288 ◽

Cited By ~ 13

Author(s):

Suman Jangra ◽

Sunita Devi ◽

Vijay K. Tomer ◽

Vinod Chhokar ◽

Surender Duhan

Keyword(s):

Drug Release ◽

Mesoporous Silica ◽

Release Kinetics ◽

Antimicrobial Property ◽

Controlled Drug Release ◽

Silver Sulfadiazine ◽

Ordered Mesoporous Silica ◽

Drug Release Kinetics ◽

Ordered Mesoporous ◽

Kinetics Of

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Eudragit S-100 coated sodium alginate microspheres of naproxen sodium: Formulation, optimization and in vitro evaluation / Alginatne mikrosfere naproksen natrija obložene Eudragitom S-100: Priprava, optimizacija i in vitro vrednovanje

Acta Pharmaceutica ◽

10.2478/v10007-012-0034-x ◽

2012 ◽

Vol 62 (4) ◽

pp. 529-545 ◽

Cited By ~ 23

Author(s):

Anuj Chawla ◽

Pooja Sharma ◽

Pravin Pawar

Keyword(s):

Drug Release ◽

Sodium Alginate ◽

Naproxen Sodium ◽

Drug Loading ◽

Size Analysis ◽

Scanning Calorimetry ◽

Sem Images ◽

S 100 ◽

Eudragit S 100

The aim of the study was to prepare site specific drug delivery of naproxen sodium using sodium alginate and Eudragit S-100 as a mucoadhesive and pH-sensitive polymer, respectively. Core microspheres of alginate were prepared by a modified emulsification method followed by cross-linking with CaCl2, which was further coated with the pH dependent polymer Eudragit S-100 (2.5 or 5 %) to prevent drug release in the upper gastrointestinal environment. Microspheres were characterized by FT-IR spectroscopy, X-ray diffraction, differential scanning calorimetry and evaluated by scanning electron microscopy, particle size analysis, drug loading efficiency, in vitro mucoadhesive time study and in vitro drug release study in different simulated gastric fluids. Stability studies of the optimized formulation were carried out for 6 months. SEM images revealed that the surface morphology was rough and smooth for core and coated microspheres, respectively. Core microspheres showed better mucoadhesion compared to coated microspheres when applied to the mucosal surface of freshly excised goat colon. The optimized batch of core microspheres and coated microspheres exhibited 98.42 ± 0.96 and 95.58 ± 0.74 % drug release, respectively. Drug release from all sodium alginate microsphere formulations followed Higuchi kinetics. Moreover, drug release from Eudragit S-100 coated microspheres followed the Korsmeyer-Peppas equation with a Fickian kinetics mechanism. Stability study suggested that the degradation rate constant of microspheres was minimal, indicating 2 years shelf life of the formulation.

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Liquid crystalline polyureas with oligo(ethylene glycol) sequences

e-Polymers ◽

10.1515/epoly.2010.10.1.1425 ◽

2010 ◽

Vol 10 (1) ◽

Author(s):

Shahram Mehdipour-Ataei ◽

Leila Akbarian-Feizi

Keyword(s):

Liquid Crystalline ◽

Spectroscopic Method ◽

Polymerization Reaction ◽

X Ray Diffraction ◽

Subsequent Reaction ◽

Scanning Calorimetry ◽

Polar Solvents ◽

X Ray ◽

H Nmr ◽

Ft Ir

AbstractA diamine monomer containing ester, amide and ether functional groups was prepared and its polymerization reaction with different diisocyanates to give main chain poly(ester amide ether urea)s was investigated. The monomer was synthesized via reaction of terephthaloyl chloride with 4-hydroxybenzoic acid and subsequent reaction of the resulted diacid with 1,8-diamino-3,6-dioxaoctane. The polymers were characterized by FT-IR and 1H-NMR spectroscopic method and elemental analysis. The resulting polymers exhibited excellent solubility in polar solvents. Crystallinity of the resulted polymers was evaluated by wide-angle X-ray diffraction (WXRD) method, and they exhibited semi-crystalline patterns. The glass transition temperatures (Tg) of the polymers determined by differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) were in the range of 88-112 °C. The temperatures for 10% weight loss (T10) from their thermogravimetric analysis (TGA) curves were found to be in the range of 297-312 °C in air. Also the prepared polyureas showed liquid crystalline character.

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