The PROPEL™ sinus implant maintains patency and locally delivers steroid to the sinus mucosa in patients 18 years and older following sinus surgery.
The PROPEL™ family of sinus implants is the first and only FDA (Food & Drug Administration) approved steroid eluting sinus implant.1 PROPEL™ sinus implants come in three sizes, allowing ENT (Ear, Nose & Throat) physicians to select the best option that conforms to the anatomical needs of their patients.2–4
PROPEL™ sinus implants feature an innovative two-in-one mechanism that opens in the sinuses while delivering MF, a potent corticosteroid, directly where it is needed.2–4
Mometasone furoate delivers a combination of potency and safety.
| Topical corticosteroid | Lipophilicity‡,6 | Potency (receptor affinity)†,7 | Systemic bioavailability‡,8 |
|---|---|---|---|
| Dexamethasone | Very low (<1.0) | Very low (100) | High (76%) |
| Triamcinolone (Kenalog) | Low (1.0) | Low (233) | Medium (46%) |
| Budesonide | Low (1.6) | Intermediate (935) | Medium (34%) |
| Mometasone furoate | High (20.0) | High (2,300) | Very low (<1%) |
PROPEL™ sinus implants are clinically proven to maintain patency and improve patient outcomes following endoscopic sinus surgery by targeting inflammation, the underlying cause of chronic rhinosinusitis.
† Lipophilicity numbers normalized relative to triamcinolone acetonide. ‡ As measured by relative receptor binding affinity compared to dexamethasone, which is set to a value of 100. Higher values designate greater potency.