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Mesoporous silica nanoparticles (MSNs) are greatly appealing for efficient drug delivery due to their excellent drug loading capacities.
Indomethacin (IDM), an anionic drug, was chosen as a model drug to evaluate the drug loading capacities of CPβCDs.
The tunable structures of CPβCDs make them promising drug carriers with superior drug loading capacities and controllable drug release abilities.
The synthesis of LDH can be conducted via two major chemical routes, which are co-precipitation or ion-exchange method; both methods can be utilized for drug intercalation and have been reported to have high drug loading capacities [21].
Finally, the drug loading capacities of the magnetite and tumor dual-targeting hollow P MBAAm-co-MAA) microsP MBAAm-co-MAAir releasing deP MBAAm-co-MAA values were investigated with doxorubicin hydrochloride (DXR) as an anticancer drug microspheres
The co-delivery of DOX and GEM was achieved for the first time via an inorganic nanocarrier, possessing a zero-premature leakage behavior as well as drug loading capacities seven times higher than polymersome NPs.
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The carrier/drug incompatibility will result in not only low drug loading capacity, but also limited stability of the drug-loaded micelles.
Drug loading capacity.
The drug loading capacity was assessed using ketoprofen and paracetamol.
The drug loading capacity and encapsulation efficiency are calculated as follows: drug loading capacity = weight of etoposide in ECCNSs weight of ECCNSs × 100%%.
The drug loading capacity and drug loading efficiency of polymeric micelles were 8 and 44 %, respectively (Table 2).
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