Dependence therapeutic effects of intranasal glucocorticoids on deposition in nasal cavities
Main Article Content
Abstract
Intranasal glucocorticoids are the treatment of choice in the therapy of rhinitis. The differences in efficiency of particular medications proven by therapeutic index may result from differences in composition of particular formulations as well as from diverse deposition in nasal cavities. All intranasal medications deposited mainly on the anterior part of inferior turbinate. Deposited also on the anterior part of the middle nasal turbinate, marginally embracing a fragment of the central part of this turbinate as well together with deposition in the middle and superior nasal meatus reaching the region of nasal ceiling and olfactory field. Mometasone furoate preparation deposited on the anterior part of the inferior turbinate and central part of this turbinate alike. The area of mucous membrane of lateral wall of nasal cavity on which mometasone furoate deposited was similar to the area achieved after the application of fluticasone propionate preparation but much greater than in the case of fluticasone furoate. The interaction of the air flow with the layer of deposited fluid plays a major role in the deposition of the drug in the nasal cavity, therefore it is so important that the drug does not drain by gravity but remains at the site of deposition which may be reinforced by thixotropic properties of the preparation.
Downloads
Article Details
Copyright: © Medical Education sp. z o.o. This is an Open Access article distributed under the terms of the Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). License (https://creativecommons.org/licenses/by-nc/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Address reprint requests to: Medical Education, Marcin Kuźma (marcin.kuzma@mededu.pl)
References
2. Bousquet J., van Cauwenberge P., Khaltaev N.; ARIA Workshop Group: World Health Organization: Allergic rhini-tis and its impact on asthma. J. Allergy Clin. Immunol. 2001, 108(5 supl.): S147-S334.
3. Brożek J.L., Bousquet J., Baena-Cagnani C.E. et al.: Allergic rhinitis and its impact on asthma (ARIA) guidelines: 2010 revison. J. Allergy Clin. Immunol. 2010, 126: 466-476.
4. Fokkens W.J., Lund V.J., Mullol J. et al.; EPOS 2012: European position paper on rhinosinusitis and nasal polyps 2012. A summary for otorhinolaryngologists. Rhinology 2012, 50(1): 1-12.
5. Arcimowicz M., Buczyłko K., Duda R. et al.: Polskie Standardy Leczenia Nieżytów Nosa (PoSLeNN). Alergol. Pol. 2013: S1.
6. Jurkiewicz D., Rapiejko P.: Alergiczny nieżyt nosa. W: Niemczyk K., Jurkiewicz D., Składzień J. et al. (red.): Otolaryngologia kliniczna, t. 2. Medipage, Warszawa 2015: 780-783.
7. Rapiejko P.: Kompleksowe leczenie alergicznego nieżytu nosa. Alergoprofil 2015, 11(1): 6-19.
8. Derendorf H., Meltzer E.O.: Molecular and clinical pharmacology of intranasal corticosteroids and therapeutic implications. Allergy 2008, 63: 1292-1300.
9. Schäfer T., Schnoor M., Wagenmann M. et al.: Therapeutic Index (TIX) for intranasal corticosteroids in the treatment of allergic rhinitis. Rhinology 2011, 49: 272-280.
10. Samoliński B., Nowicka A., Wojas O. et al.: Intranasal glucocorticosteroids – not only in allergic rhinitis in the 40th anniversary of intranasal glucocorticosteroids’ introduction. Otolaryngol. Pol. 2014, 68: 51-64.
11. Samoliński B., Krzych-Fałta E.: Efektywność działania donosowych glikokortykosteroidów w alergicznym nieżycie nosa mierzona indeksem terapeutycznym. Alergoprofil 2015, 11(1): 3-5.
12. Rapiejko P., Wojdas A., Ratajczak J., Szczygielski K., Jurkiewicz D.: Technika podawania leków donosowo. Pol. Merk. Lek. 2005, 19(111): 400-402.
13. Platt M.: Pharmacotherapy for allergic rhinitis. Int. Forum Allergy Rhinol. 2014, 4(supl. 2): 35-40.
14. Samoliński B., Rapiejko P.: Odpowiedź późna po donosowej próbie prowokacyjnej z alergenem. Postępy Dermatologii i Alergologii 2010, XXVII(3): 173-176.
15. Wang D.Y., Raza M.T., Gordon B.R.: Control of nasal obstruction in perennial allergic rhinitis. Curr. Opin. Allergy Clin. Immunol. 2004, 4(3): 165-170.
16. Sharpe S.A., Sandweiss V., Tuazon J. et al.: Comparison of the flow properties of aqueous suspension corticosteroid nasal sprays under differing sampling conditions. Drug Dev. Ind. Pharm. 2003, 29(9): 1005-1012.
17. Castile J., Cheng Y.H., Simmons B. et al.: Development of in vitro models to demonstrate the ability of PecSys®, an in situ nasal gelling technology, to reduce nasal run-off and drip. Drug Dev. Ind. Pharm. 2013, 39(5): 816-824.
18. Kimbell J.S., Segal R.A., Asgharian B. et al.: Characterization of deposition from nasal spray devices using a computational fluid dynamics model of the human nasal passages. J. Aerosol. Med. 2007, 20: 59-74.
19. Djupeslund P.G.: Nasal drug delivery devices: characteristics and performance in a clinical perspective – a review. Drug Deliv. Transl. Res. 2013, 3: 42-62.
20. Djupesland P.G., Skretting A.: Nasal deposition and clearance in man: comparison of a bidirectional powder device and a traditional liquid spray pump. J. Aerosol Med. Pulm. Drug Del. 2011, 25(5): 280-289.