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Hydroxypropylcellulose-flurbiprofen conjugates: design, characterization, anti-inflammatory activity and enhanced bioavailability.


ABSTRACT: Herein, we report novel macromolecular prodrugs (MPDs) of flurbiprofen (FLB) onto a cellulose ether, hydroxypropylcellulose (HPC). The FLB was activated with a powerful acylation reagent carbonyldiimadazole (CDI) in N,N' dimethylacetamide (DMAc) solvent at room temperature. Imidazolide of FLB generated in situ reacts at 80 °C for 24 h with pre-dissolved HPC to prepare HPC-FLB conjugates. The resultant MPDs of FLB showed moderate to high degree of substitution (DS: 0.35-1.3) with good yield (70-82%). Structures were thoroughly characterized using FTIR, UV and NMR spectroscopic analyses. The pharmacokinetic studies showed that the t1/2 and tmax values of FLB from HPC-FLB conjugate were increased substantially as compare to standard FLB indicates enhanced bioavailability of drug after conjugate formation. Remarked anti-inflammatory activity of the HPC-FLB conjugate was also observed.

SUBMITTER: Hussain MA 

PROVIDER: S-EPMC7335720 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Hydroxypropylcellulose-flurbiprofen conjugates: design, characterization, anti-inflammatory activity and enhanced bioavailability.

Hussain Muhammad Ajaz MA   Shad Iqra I   Malik Iram I   Amjad Fasiha F   Kausar Tehreem T   Kamran   Sher Muhammad M   Tahir Muhammad Nawaz MN   Ullah Nisar N   Ashraf Muhammad M   Bukhari Syed Nasir Abbas SNA  

Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society 20200623 7


Herein, we report novel macromolecular prodrugs (MPDs) of flurbiprofen (FLB) onto a cellulose ether, hydroxypropylcellulose (HPC). The FLB was activated with a powerful acylation reagent carbonyldiimadazole (CDI) in <i>N,N</i>' dimethylacetamide (DMAc) solvent at room temperature. Imidazolide of FLB generated <i>in situ</i> reacts at 80 °C for 24 h with pre-dissolved HPC to prepare HPC-FLB conjugates. The resultant MPDs of FLB showed moderate to high degree of substitution (DS: 0.35-1.3) with go  ...[more]

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