The phrase "air pouch model" is correct and usable in written English.
It can be used in contexts related to scientific, engineering, or design discussions where a model or concept involving an air pouch is being described.
Example: "The air pouch model demonstrates how air can be utilized to enhance buoyancy in various aquatic designs."
Alternatives: "air chamber model" or "air bladder model".
Investigations were performed using carrageenan induced rat air pouch model.
Both compounds exhibit anti-inflammatory effect in the dorsal air pouch model of inflammation as shows by inhibition of PGE2 secretion.
The optimized formulation was fabricated into the transdermal patch and in-vivo pharmacokinetic and pharmacodynamic study (subcutaneous air pouch model) was carried out.
In the rat air pouch model, oral dosing of CJ-13,610 and zileuton resulted in selective inhibition 5-LO Xactivity from pouch exudate and ex vivo rat whole blood with similar potency to in vitro assay.
The anti-inflammatory effects of antifolates were estimated using the murine air pouch model, in which a BALB/c mouse was intraperitoneally injected with MX-68 or MTX once a week for 3 weeks.
The introduction of 3-arylmethyl, 3-aryloxy and 3-arylthio moieties into a 6-methylsulfonylindole framework using rational drug design led to potent, selective COX-2 inhibitors having efficacy in a rat carrageenan air pouch model.
This was investigated in vivo using a mouse air-pouch model of inflammation.
The M1/M2 phenotypic polarization profile of macrophages was investigated in vivo using a rodent air-pouch model.
The in vivo effect on leukocyte migration of these compounds was investigated by using the mouse air-pouch model of local inflammation.
In order to investigate if the necrotic cell death caused by activated NLRP3 induced a neutrophilic inflammatory response, we performed neutrophil infiltration assays using an air-pouch model.
Recently, two separate studies demonstrated anti-inflammatory properties of PGD2 in an air-pouch model of inflammation induced by monosodium urate monohydrate crystals [ 13, 51].
