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Related Concept Videos

Ophthalmic Drug Delivery Systems01:23

Ophthalmic Drug Delivery Systems

Ophthalmic drug delivery faces major limitations due to poor absorption across the corneal membrane. This process is primarily driven by diffusion and is influenced by two main factors: the physicochemical properties of the drug and tear drainage. Most ophthalmic drugs, such as pilocarpine, epinephrine, atropine, and local anesthetics, are weak bases. They are typically formulated at an acidic pH to enhance chemical stability. However, this leads to high ionization, reducing their ability to...
Drug Delivery: Enteral Route01:18

Drug Delivery: Enteral Route

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.
Drugs in...
Drug Delivery: Miscellaneous Routes01:22

Drug Delivery: Miscellaneous Routes

Drug delivery methods like oral inhalation, nasal sprays, transdermal patches, eye drops, intravitreal injection,  and rectal administration provide localized effects with reduced toxicity.
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs through the...
Oral Drug Delivery Systems: Introduction01:23

Oral Drug Delivery Systems: Introduction

Oral drug delivery is the most common route of administration due to its convenience, cost-effectiveness, and high patient compliance. It enables precise formulation to ensure proper drug dosage and bioavailability. The development of oral dosage forms considers drug properties such as solubility, stability, and absorption to optimize therapeutic efficacy.Tablets, capsules, liquids, and chewable formulations enhance drug stability, mask undesirable tastes, and improve patient experience.
Oral Drug Delivery Systems: Continuous-Release Systems01:26

Oral Drug Delivery Systems: Continuous-Release Systems

Continuous-release drug delivery systems offer a strategic approach to maintaining therapeutic drug levels over extended periods following oral administration. By modulating the release rate of active pharmaceutical ingredients, these systems minimize fluctuations in plasma concentrations, which enhances clinical efficacy and reduces the need for frequent dosing. Such characteristics make them particularly advantageous in managing chronic diseases where patient adherence and stable drug...
Drug Delivery: Overview01:16

Drug Delivery: Overview

The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the gastrointestinal...

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Related Experiment Video

Updated: May 16, 2026

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
09:52

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity

Published on: March 16, 2018

Formulations for trans-tympanic antibiotic delivery.

Xiaojuan Khoo1, Emmanuel J Simons, Homer H Chiang

  • 1Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Biomaterials
|November 14, 2012
PubMed
Summary

This study presents a novel hydrogel drug delivery system for prolonged trans-tympanic antibiotic administration. This system enhances ciprofloxacin permeability through the tympanic membrane, offering a potential treatment for middle ear infections.

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Area of Science:

  • Otolaryngology
  • Drug Delivery Systems
  • Biomaterials Science

Background:

  • Acute otitis media (AOM) and other middle ear diseases often require effective antibiotic treatment.
  • Current treatment methods may face challenges with drug penetration and sustained release.
  • Developing advanced drug delivery systems is crucial for improving ototopical therapies.

Purpose of the Study:

  • To develop and evaluate a novel hydrogel-based drug delivery system for prolonged trans-tympanic antibiotic delivery.
  • To assess the efficacy of chemical permeation enhancers (CPEs) in increasing ciprofloxacin permeability across the intact tympanic membrane (TM).
  • To investigate the safety and efficacy of the CPE-hydrogel formulation for ototopical delivery.

Main Methods:

  • Formulation of a hydrogel (poloxamer 407) incorporating chemical permeation enhancers (bupivacaine, limonene, sodium dodecyl sulfate).
  • Evaluation of ciprofloxacin permeability through the intact tympanic membrane using the CPE-hydrogel system.
  • In vivo assessment of the CPE-hydrogel formulation's effects on auditory thresholds and tissue response.

Main Results:

  • The CPE-hydrogel formulation significantly increased tympanic membrane permeability to ciprofloxacin.
  • The hydrogel effectively maintained the formulation at the tympanic membrane site.
  • In vivo studies demonstrated minimal adverse effects on auditory thresholds and tissue response.

Conclusions:

  • CPE-hydrogel formulations show significant potential for sustained, single-dose trans-tympanic delivery of ciprofloxacin.
  • This drug delivery system offers a promising approach for treating acute otitis media and other middle ear infections.
  • Further research into CPE-hydrogel formulations could advance ototopical antibiotic delivery strategies.