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. Author manuscript; available in PMC: 2022 Oct 10.
Published in final edited form as: J Control Release. 2021 Sep 2;338:593–609. doi: 10.1016/j.jconrel.2021.08.059

Table 1.

Summary of bioactivities of metal-based CO-RMs in vivo via oral administration

Compound Activity Animal model Dosage COHb (%) Side product control Ref
CORM-2 gastric injury rats 5 mg/kg 10 mg/kg 1.6% (5mg/kg) 2.2% (50mg/kg) RuCl3 [137]
CORM-A1 cerebrovascular dysfunction piglets 2 mg/kg NA B(OH)3 [128]
ALF-186 acute toxicity evaluation mice 500 mg/kg 35%-40% NA [150]
CORM-401 obesity mice 15 mg/kg 30 mg/kg 2.5% 4.5% iCORM [139]
HYCO-4 inflammation mice 3 mg/kg 4% NA [141]
HYCO-10 inflammation mice 3 mg/kg 2% NA [141]
HYCO-3 inflammation mice 40 mg/kg 5% NA [143]
HYCO-6 Skin wound mice 40 mg/kg 2% NA [145]
HYCO-3 HYCO-13 Psoriasis, multiple sclerosis mice 25 mg/kg 2% 5% NA [145]
CAI-CORM rheumatoid arthritis rats 10-100 mg/kg NA NA [165]
M-OCORS colitis mice 2 tablets 0.69% abrogated - CORM-2 [158]
M-OCORS postoperative ileus mice 20 tablets 5.2% NA [161]
SMA/CORM2 Rheumatoid Arthritis mice 20 mg/kg NA NA [162]