Formulation, In-vitro and In-vivo Evaluation of Semi-Interpenetrating Polymer Network (semi-IPN) Microspheres of Ketorolac Tromethamine

2013 ◽  
Vol 01 (03) ◽  
pp. 48-54 ◽  
Author(s):  
A. A. Kassem ◽  
◽  
M. A. Marzouk ◽  
Sh. A. El- Adawy ◽  
A.M. Dawaba
2014 ◽  
Vol 22 (4) ◽  
pp. 349-359 ◽  
Author(s):  
Amal El Sayeh F. Abou el Ela ◽  
Maha A. Hassan ◽  
Dalia A. El- Maraghy

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2674
Author(s):  
Giulia Morello ◽  
Alessandro Polini ◽  
Francesca Scalera ◽  
Riccardo Rizzo ◽  
Giuseppe Gigli ◽  
...  

In recent years, growing attention has been directed to the development of 3D in vitro tissue models for the study of the physiopathological mechanisms behind organ functioning and diseases. Hydrogels, acting as 3D supporting architectures, allow cells to organize spatially more closely to what they physiologically experience in vivo. In this scenario, natural polymer hybrid hydrogels display marked biocompatibility and versatility, representing valid biomaterials for 3D in vitro studies. Here, thermosensitive injectable hydrogels constituted by chitosan and pectin were designed. We exploited the feature of chitosan to thermally undergo sol–gel transition upon the addition of salts, forming a compound that incorporates pectin into a semi-interpenetrating polymer network (semi-IPN). Three salt solutions were tested, namely, beta-glycerophosphate (βGP), phosphate buffer (PB) and sodium hydrogen carbonate (SHC). The hydrogel formulations (i) were injectable at room temperature, (ii) gelled at 37 °C and (iii) presented a physiological pH, suitable for cell encapsulation. Hydrogels were stable in culture conditions, were able to retain a high water amount and displayed an open and highly interconnected porosity and suitable mechanical properties, with Young’s modulus values in the range of soft biological tissues. The developed chitosan/pectin system can be successfully used as a 3D in vitro platform for studying tissue physiopathology.


Pharmaceutics ◽  
2011 ◽  
Vol 3 (4) ◽  
pp. 954-970 ◽  
Author(s):  
Guadalupe Nava ◽  
Elizabeth Piñón ◽  
Luis Mendoza ◽  
Néstor Mendoza ◽  
David Quintanar ◽  
...  

2021 ◽  
pp. 103590
Author(s):  
Muhammad Suhail ◽  
Jia-Yu Liu ◽  
Wan-Chu Hsieh ◽  
Yu-Wen Lin ◽  
Muhammad Usman Minhas ◽  
...  

2014 ◽  
Vol 69 ◽  
pp. 514-522 ◽  
Author(s):  
Raghavendra V. Kulkarni ◽  
Foram S. Patel ◽  
H.M. Nanjappaiah ◽  
Akram A. Naikawadi

Gels ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 167
Author(s):  
Muhammad Suhail ◽  
Yi-Han Hsieh ◽  
Yu-Fang Shao ◽  
Muhammad Usman Minhas ◽  
Pao-Chu Wu

Ketorolac tromethamine is a non-steroidal anti-inflammatory drug used in the management of severe pain. The half-life of Ketorolac tromethamine is within the range of 2.5–4 h. Hence, repeated doses of Ketorolac tromethamine are needed in a day to maintain the therapeutic level. However, taking several doses of Ketorolac tromethamine in a day generates certain complications, such as acute renal failure and gastrointestinal ulceration. Therefore, a polymeric-controlled drug delivery system is needed that could prolong the release of Ketorolac tromethamine. Therefore, in the current study, pH-responsive carbopol 934/sodium polystyrene sulfonate-co-poly(acrylic acid) (CP/SpScPAA) hydrogels were developed by the free radical polymerization technique for the controlled release of Ketorolac tromethamine. Monomer acrylic acid was crosslinked with the polymers carbopol 934 and sodium polystyrene sulfonate by the cross-linker N′,N′-methylene bisacrylamide. Various studies were conducted to evaluate and assess the various parameters of the fabricated hydrogels. The compatibility of the constituents used in the preparation of hydrogels was confirmed by FTIR analysis, whereas the thermal stability of the unreacted polymers and developed hydrogels was analyzed by TGA and DSC, respectively. A smooth and porous surface was indicated by SEM. The crystallinity of carbopol 934, sodium polystyrene sulfonate, and the prepared hydrogels was evaluated by PXRD, which revealed a reduction in the crystallinity of reactants for the developed hydrogels. The pH sensitivity of the polymeric hydrogel networks was confirmed by dynamic swelling and in vitro release studies with two different pH media i.e., pH 1.2 and 7.4, respectively. Maximum swelling was exhibited at pH 7.4 compared to pH 1.2 and, likewise, a greater percent drug release was perceived at pH 7.4. Conclusively, we can demonstrate that the developed pH-sensitive hydrogel network could be employed as a suitable carrier for the controlled delivery of Ketorolac tromethamine.


2016 ◽  
Vol 18 (3) ◽  
pp. 654-670 ◽  
Author(s):  
Famida G. Hoosain ◽  
Yahya E. Choonara ◽  
Pradeep Kumar ◽  
Lomas K. Tomar ◽  
Charu Tyagi ◽  
...  

2009 ◽  
Vol 23 (1) ◽  
pp. 26-34 ◽  
Author(s):  
Rajesh Dubey ◽  
Madhusudhan Bommagani ◽  
Vobalaboina Venkateswarlu ◽  
Ramesh Mullangi ◽  
Harinder R. Karnati ◽  
...  

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