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Related Concept Videos

Inhaled Medications01:23

Inhaled Medications

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Inhaled medications are crucial for managing chronic obstructive pulmonary disease (COPD) and asthma. They are essential for effective treatment and control, ensuring optimal respiratory health and well-being. Inhaled medication delivers drugs directly to the lungs, providing a rapid onset of action and reducing systemic side effects compared to oral or injectable medications. Three primary types of inhalation devices are used to administer these medications: nebulizers, metered-dose inhalers...
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Inhalational Anesthetics: Overview01:20

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Inhalation anesthetics are drugs that induce general anesthesia upon inhalation. They work by increasing the sensitivity of GABAA receptors or inhibiting NMDA receptors, leading to a decrease in central nervous system activity. The depth of anesthesia can be rapidly adjusted by changing the concentration of the inhaled gas. Some common examples of inhalational anesthetics include volatile liquids like isoflurane, desflurane, sevoflurane and gases like xenon and nitrous oxide. Isoflurane, a...
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Additional Routes of Drug Administration01:18

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Choosing the appropriate route of drug administration is significantly influenced by two key factors: the therapeutic objectives and the inherent properties of the drug being used.
Administering drugs via inhalation allows for the direct delivery of gaseous, volatile substances or droplets to different parts of the respiratory tract. One of the advantages of the inhalation route is the rapid absorption of drugs into the circulatory system, which is possible because of the large surface area of...
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Drug Delivery: Miscellaneous Routes01:22

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Drug delivery methods like oral inhalation, nasal sprays, transdermal patches, eye drops, intravitreal injection,  and rectal administration provide localized effects with reduced toxicity.
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The enteral drug administration involves three primary routes: oral, sublingual, and buccal. Oral ingestion is the most prevalent, safe, economical, and convenient method for drug administration. However, it has certain drawbacks, including limited absorption due to the drug's low water solubility or poor membrane permeability, possible emesis from GI mucosa irritation, destruction of drugs by digestive enzymes or low gastric pH, and irregular absorption along with food or other drugs.
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Related Experiment Video

Updated: Jan 1, 2026

Dry Powder and Nebulized Aerosol Inhalation of Pharmaceuticals Delivered to Mice Using a Nose-only Exposure System
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Particle engineered mannitol for carrier-based inhalation - A serious alternative?

Nancy Hertel1, Gudrun Birk2, Regina Scherließ1

  • 1Department of Pharmaceutics and Biopharmaceutics, Kiel University, Grasweg 9a, 24118 Kiel, Germany.

International Journal of Pharmaceutics
|December 18, 2019
PubMed
Summary

Particle engineered mannitol shows promise as a dry powder inhalation (DPI) carrier, matching or exceeding lactose performance. Mannitol blends offer uniform dosing and comparable or improved respirable fractions for active pharmaceutical ingredients (APIs).

Keywords:
Aerodynamic performanceAlpha-lactose (PubChem CID: 84571)Budesonide (PubChem CID: 5281004)Dry powder inhalationLactoseMannitol (PubChem CID: 6251)Physico-chemical characterisationSalbutamol sulphate (PubChem CID: 39859)

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Area of Science:

  • Pharmaceutical Technology
  • Drug Delivery Systems
  • Materials Science

Background:

  • Dry powder inhalation (DPI) formulations commonly use lactose as a carrier for micronized active pharmaceutical ingredients (APIs).
  • Research into alternative DPI carriers has been ongoing, but few have reached the market.

Purpose of the Study:

  • To evaluate spray-granulated mannitol as a potential alternative carrier for DPI formulations.
  • To compare the performance of mannitol-based blends against traditional lactose carriers.

Main Methods:

  • Preparation of DPI blends with varying concentrations (0.1-4%) of two different APIs using lactose and spray-granulated mannitol carriers.
  • Characterization of physical properties (particle size, morphology, density, flowability) and dosing behavior.
  • Aerodynamic performance assessment using two inhaler devices and varying flow rates.

Main Results:

  • Mannitol blends demonstrated good flowability, enabling uniform dosing across API concentrations.
  • Linear dose delivery was observed with increasing API concentrations.
  • Respirable fractions for mannitol blends were comparable to lactose for salbutamol sulphate and higher for budesonide.

Conclusions:

  • Particle-engineered mannitol is a viable alternative carrier for DPI formulations.
  • Mannitol carriers support consistent dosing and efficient drug delivery, comparable or superior to lactose.