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Metered-dose inhaler

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File:ProAirHFA.png
ProAir-HFA
Albuterol Sulfate(US)

A metered-dose inhaler (MDI) is a device that delivers a specific amount of medication to the lungs, in the form of a short burst of aerosolized medicine that is inhaled by the patient. It is the most commonly used delivery system for treating asthma, chronic obstructive pulmonary disease (COPD) and other respiratory diseases. The medication in a metered dose inhaler is most commonly a bronchodilator, corticosteroid or a combination of both for the treatment of asthma and COPD. Other medications less commonly used but also administered by MDI are mast cell stabilizers, such as (cromoglicate or nedocromil).

Description

deep drawn MDI canister made by Pressteck (Italy)

A metered-dose inhaler consists of three major components; the canister which is produced in aluminium or stainless steel by means of deep drawing, where the formulation resides; the metering valve, which allows a metered quantity of the formulation to be dispensed with each actuation; and an actuator (or mouthpiece) which allows the patient to operate the device and directs the aerosol into the patient's lungs.[1],[2] The formulation itself is made up of the drug, a liquefied gas propellant and, in many cases, stabilising excipients. The actuator contains the mating discharge nozzle and generally includes a dust cap to prevent contamination.

To use the inhaler the patient presses down on the top of the canister, with their thumb supporting the lower portion of the actuator. Actuation of the device releases a single metered dose of the formulation which contains the medication either dissolved or suspended in the propellant. Breakup of the volatile propellant into droplets, followed by rapid evaporation of these droplets, results in the generation of an aerosol consisting of micrometer-sized medication particles that are then inhaled.[3]

Uses

Metered-dose inhalers are only one type of inhaler, but they are the most commonly used type. The replacement of chlorofluorocarbons propellants with hydrofluoralkanes resulted in the redesign of metered-dose inhalers in the 1990s. For one variety of beclomethasone inhaler, this redesign resulted in considerably smaller aerosol particles being produced, and led to an increase of potency by a factor of 2.6[4].

  • Asthma inhalers contain a medication that treats the symptoms of asthma.
  • Dry powder inhalers involve micronised powder often packaged in single dose quantities in blisters or gel capsules containing the powdered medication to be drawn into the lungs by the user's own breath. These systems tend to be more expensive than the MDI, and patients with severely compromised lung function, such as occurs during an asthma attack, may find it difficult to generate enough airflow to get good function from them.
  • A nicotine inhaler allows cigarette smokers to get nicotine without using tobacco, much like nicotine gum or a nicotine patch. Nicotine inhalers that are marketed as nicotine replacement therapy should not be confused with electronic cigarettes, which produce vapour and which are marketed mainly as devices that smokers can use in non-smoking areas.

History

Before the invention of the MDI asthma medication was delivered using a squeeze bulb nebulizer which was fragile and unreliable.[5] The relatively crude nature of these devices also meant that the particles that they generated were relatively large, too large for effective drug delivery to the lungs.[2] Nonetheless these nebulisers paved the way for inhaltion drug delivery providing the inspiration for the MDI.

MDI's were first developed in 1955 by Riker Laboratories, now a subsidiary of 3M Healthcare.[5] At that time MDI's represented a convergence of two relatively new technologies, the CFC propellant and the Meshburg metering valve which was originally designed for dispensing perfume.[6] The initial design by Riker used a glass canister coated with a vinyl plastic to improve its resilience.[5] By 1956 Riker had developed two MDI based products, the Medihaler-Ept containing epinephrin and the Medihaler-Iso containing Isoprenaline.[2] Both products are agonists which provide short term relief from asthma symptoms and have now largely been replaced in asthma treatment by salbutamol which is more selective.

Spacers

Main article: Asthma spacer

Metered-dose inhalers are sometimes used with add-on devices referred to as holding chambers or spacers, which are tubes attached to the inhaler that act as a reservoir or holding chamber and reduce the speed at which the aerosol enters the mouth. They serve to hold the medication that is sprayed by the inhaler. This makes it easier to use the inhaler and helps ensure that more of the medication gets into the lungs instead of just into the mouth or the air. With proper use, a spacer can make an inhaler somewhat more effective in delivering medicine.[7]

Spacers can be especially helpful to adults and children who find a regular metered dose inhaler hard to use. People who use corticosteroid inhalers should use a spacer to prevent getting the medicine in their mouth, where oral yeast infections and dysphonia can occur[8].

Lifespan and replacement

A metered dose inhaler contains enough medication for a certain number of actuations (or puffs) which is printed on the canister. Even though the inhaler may continue to work beyond that number of uses, the amount of medication delivered may not be correct. It is important to keep track of the number of times an inhaler was used, so that it can be replaced after its recommended number of uses. For this reason, several regulatory authorities have requested that manufacturers add a dose counter or dose indicator to the actuator. Several inhalation products are now sold with a dose counter-actuator. Depending on the manufacturer and the product, inhalers are sold as a complete unit or the individual canister as a refill prescription.

Propellants

CFC-free Asthalin HFA inhaler made by Cipla (India)

One of the most crucial components of a MDI is its propellant. The propellant provides the force to generate the aerosol cloud and is also the medium in which the active component must be suspended or dissolved. Propellants in MDIs typically make up more than 99 % of the delivered dose,[9] so it is the properties of the propellant that dominate more than any other individual factor. This is often overlooked in literature and in industry because so few propellants are used and their contribution is often taken for granted. Suitable propellants must pass a stringent set of criteria, they must:

  • have a boiling point in the range -100 to +30°C [10]
  • have a density of approximately 1.2 to 1.5 g cm−3 (approximately that of the drug to be suspended or dissolved)[9]
  • have a vapour pressure of 40 to 80 psig [11]
  • have no toxicity to the patient [9][11]
  • be non flammable [9][11]
  • be able to dissolve common additives. Active ingredients should be either fully soluble or fully insoluble.[9]

Chlorofluorocarbons (CFCs)

In the early days of MDIs the most commonly used propellants were the chlorofluorocarbons CFC-11, CFC-12 and CFC-114.

Transition to HFA propellants

In the United States starting from December 2008 inhalers containing chlorofluorocarbons, as a form of propellant to deliver the medication, will be discontinued for hydro-fluoroalkane-pressurized metered dose inhalers (HFA pMDI's).[citation needed] As governed by the 1987 Montreal Protocol on Substances that Deplete the Ozone Layer, all inhalers that contain CFCs are being discontinued with the target year 2010 under the auspices of the UN Environment Programme.[12] As a consequence of the Montreal protocol, the first companies to patent an inhaler formulation containing HFAs are Riker for the HFA 134a in 1989 (EP372777) and Hoescht for the HFA227 in 1990 (DE3905726A1) [13]. These patents are now expired. [14]

See also

References

  1. ^ Pharmaceutical Inhalation Aerosol Technology, ed. A. J. Hickey, 2nd edition, Marcel Dekker Inc., NY, 2004.
  2. ^ a b c Swarbrick, James (2007). Encyclopedia of Pharmaceutical Technology (3rd Illustrated ed.). Informa Health Care. p. 1170. ISBN 0849393949.
  3. ^ Finlay, W. H., The Mechanics of Inhaled Pharmaceutical Aerosols: An Introduction, Academic Press, 2001.
  4. ^ Busse W, Colice G, Hannon S. CFC-BDP require 2.6 times the dose to achieve equivalent improvement in FEV1 as HFA-BDP. Am J Respir Crit Med 1998; 157:A405.
  5. ^ a b c Purewal, Tol S. (1997). Metered Dose Inhaler Technology (Illustrated ed.). Informa Health Care. ISBN 1574910655. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  6. ^ Clark, A. R (1995). "Medical Aerosol Inhalers: Past, Present, and Future". Aerosol Science and Technology. 22 (4): 374–391. doi:10.1080/02786829408959755.
  7. ^ Togger, D., & Brenner, P. (2001). Metered dose inhalers. American Journal of Nursing, 101 (10), 29.
  8. ^ ""Inhalation Aerosols: Physical and Biological Basis for Therapy"", ed. A. J. Hickey, 2nd edition, Informa Healthcare, NY, 2007.
  9. ^ a b c d e Noakes, T (2002). "Medical Aerosol Propellants". Journal of Fluorine Chemistry. 118 (1–2): 35–45. doi:10.1016/S0022-1139(02)00191-4.
  10. ^ "Ensuring Patient Care" (PDF). IPAC. Retrieved 2009-04-14. {{cite web}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  11. ^ a b c Leach, C L (1995). "Approaches and Challenges to Use Freon Propellant Replacements". Aersol Science and Technology. 22 (4): 328–334. doi:10.1080/02786829408959750.
  12. ^ "The Montreal Protocol on Substances that Deplete the Ozone Layer" (PDF). United Nations Environment Programme.
  13. ^ "Original HFA propellant related patents". Hoechst, Fisons, Riker and Boehringer Ingelheim and Virginia Commonwealth University.
  14. ^ "What is the future of HFA pMDIs? A patent-based perspective". Inhalation Magazine.
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