Literature DB >> 16464549

Acrylic/cyclodextrin hydrogels with enhanced drug loading and sustained release capability.

Ulf Siemoneit1, Christoph Schmitt, Carmen Alvarez-Lorenzo, Asteria Luzardo, Francisco Otero-Espinar, Angel Concheiro, José Blanco-Méndez.   

Abstract

The influence of the proportion of acrylamidomethyl-gamma-cyclodextrin (gamma-CD-NMA) on loading and release of the hydrophobic triamcinolone acetonide (TA) and the hydrophilic propranolol (PR) by acrylic acid hydrogels was evaluated. gamma-CD-NMA was synthesized by condensation of gamma-cyclodextrin (gamma-CD) with N-(hydroxymethyl) acrylamide. Hydrogels were prepared with gamma-CD-NMA and sodium acrylate (3 M or 4 M), using N,N'-methylen(bisacrylamide) (BIS) as cross-linker, by free radical polymerization into glass moulds of 2 mm wide and were cut as discs (10 mm diameter). gamma-CD-NMA did not modify the pH-dependent swelling of the hydrogels, but significantly increased the swelling degree in the 40:60 ethanol:water, medium in which TA can be dissolved. Hydrogels prepared with gamma-CD-NMA above 5% (w/w of total monomers) showed a remarkably higher capacity to load TA, e.g., 33 mg/g dry hydrogel versus 0.6 mg/g dry hydrogel without gamma-CD-NMA. This is explained by the formation of 1:1 inclusion complexes of TA with gamma-CD mers that overcomes the lack of interactions with the acrylic groups of the network. The release of TA in water, 0.1 N HCl, or pH 6.8 phosphate buffer was sustained for at least 24 h, whatever the pH and the composition of the medium used. In contrast, loading of PR from the water solutions was greater for hydrogels prepared with 3 M acrylate than with 4 M acrylate, irrespective to their content in gamma-CD-NMA, and in less than 2 h ca. 80% PR was released. The lower affinity of PR for the gamma-CD cavities, compared to the strong intensity of the electrostatic interactions with the acrylic acid groups, explains why the incorporation of gamma-CD-NMA did not increased the loading and control release capacity of the hydrogels of this hydrophilic drug. In summary, the copolymerisation of CD with acrylic monomers can provide highly hydrophilic pH-sensitive networks which load large amounts of hydrophobic drugs and release them in a sustained way.

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Year:  2006        PMID: 16464549     DOI: 10.1016/j.ijpharm.2005.12.046

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  7 in total

1.  Injectable PAMAM dendrimer-PEG hydrogels for the treatment of genital infections: formulation and in vitro and in vivo evaluation.

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Journal:  Mol Pharm       Date:  2011-06-20       Impact factor: 4.939

2.  Bioactive factor delivery strategies from engineered polymer hydrogels for therapeutic medicine.

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Journal:  Prog Polym Sci       Date:  2014-07       Impact factor: 29.190

3.  Cross-linked β-cyclodextrin and carboxymethyl cellulose hydrogels for controlled drug delivery of acyclovir.

Authors:  Nadia Shamshad Malik; Mahmood Ahmad; Muhammad Usman Minhas
Journal:  PLoS One       Date:  2017-02-28       Impact factor: 3.240

Review 4.  Carbohydrate-Based Host-Guest Complexation of Hydrophobic Antibiotics for the Enhancement of Antibacterial Activity.

Authors:  Daham Jeong; Sang-Woo Joo; Vijay Vilas Shinde; Eunae Cho; Seunho Jung
Journal:  Molecules       Date:  2017-08-08       Impact factor: 4.411

5.  Development of Water-Compatible Molecularly Imprinted Polymers Based on Functionalized β-Cyclodextrin for Controlled Release of Atropine.

Authors:  Yahui He; Shaomei Zeng; A M Abd El-Aty; Ahmet Hacımüftüoğlu; Woldemariam Kalekristos Yohannes; Majid Khan; Yongxin She
Journal:  Polymers (Basel)       Date:  2020-01-06       Impact factor: 4.329

Review 6.  History of cyclodextrin-based polymers in food and pharmacy: a review.

Authors:  Max Petitjean; Iñigo X García-Zubiri; José Ramón Isasi
Journal:  Environ Chem Lett       Date:  2021-04-23       Impact factor: 9.027

7.  pH responsive cross-linked polymeric matrices based on natural polymers: effect of process variables on swelling characterization and drug delivery properties.

Authors:  Fahad Naeem; Samiullah Khan; Aamir Jalil; Nazar Muhammad Ranjha; Amina Riaz; Malik Salman Haider; Shoaib Sarwar; Fareha Saher; Samrin Afzal
Journal:  Bioimpacts       Date:  2017-08-16
  7 in total

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