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The drug loading capacity was assessed using ketoprofen and paracetamol.
The drug loading capacity of particles was determined by separating the particles from the buffer solution containing free protein through centrifugation (10,000 r.p.m., 10 min).
This translates to a drug loading capacity of 56.17 and 59.17 mg/100 mg MNPs, respectively.
PCL-based micelles exhibited higher drug loading capacity than their PLLA-based counterparts.
This thermal behavior was then used to manipulate drug loading capacity and release rate.
This approach may result in improved drug loading capacity and encapsulation efficiency.
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On the basis of absorbency at 326 nm, the drug-loading capacity and drug encapsulation of HCPT-loaded nanoparticles were 7.5 and 56.8%, respectively.
HA could load Doxorubicin (DOX) via electrostatic interaction with a drug-loading capacity (DLC) of 32.5%.
The drug-loading capacity was calculated as 45±3%3 %.
These flexible surface characteristics of MSNs have high drug-loading capacity.
However, there still remain two problems waiting to be solved, i.e., low drug-loading capacity and quick drug release.
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