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Related Concept Videos

Drug Delivery: Overview01:16

Drug Delivery: Overview

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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...
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Cellular Membranes and Drug Transport01:24

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Drugs must traverse multiple biological barriers, such as multi-layered skin, single-layered intestinal epithelium, and the plasma membrane, to reach their target sites within the body. The plasma membrane, a highly structured composite of phospholipids, carbohydrates, and proteins, is the cell's protective boundary, facilitating selective substance exchange.
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Drug Delivery: Enteral Route01:18

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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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Drug Delivery: Parenteral Route01:29

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The parenteral route is a critical method of drug administration. It delivers compounds directly into the systemic circulation and bypasses the gastrointestinal tract. This approach is particularly advantageous for drugs that exhibit poor absorption or instability when administered orally.
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Transdermal Drug Delivery Systems01:18

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Transdermal drug delivery systems (TDDS) enable the controlled release of drugs across the skin into systemic circulation. They are particularly advantageous for drugs with short half-lives or narrow therapeutic indices, as they maintain consistent plasma concentrations and reduce the risk of subtherapeutic or toxic levels.TDDS are categorized into monolithic, reservoir, and mixed systems. Monolithic systems embed the drug in a polymer matrix, where diffusion governs release. Reservoir systems...
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Ophthalmic Drug Delivery Systems01:23

Ophthalmic Drug Delivery Systems

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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...
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Simultaneous drug delivery and cellular imaging using graphene oxide.

Sheng-Jen Cheng1, Hsien-Yi Chiu, Priyank V Kumar

  • 1Institute of Biomedical Engineering, College of Electrical and Computer Engineering, National Chiao Tung University, Hsinchu, Taiwan 30010. guanyu@nctu.edu.tw.

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Mildly heating graphene oxide (GO) induces blue fluorescence, enabling its use for cancer cell imaging and drug delivery without toxicity. This simple method enhances GO

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Area of Science:

  • Nanomaterials Science
  • Biomedical Engineering
  • Materials Chemistry

Background:

  • Graphene oxide (GO) is a graphene derivative with biocompatibility and a large surface area.
  • Abundant oxygen functional groups on GO facilitate its use as a nano-bio interface.
  • Current applications often require additional labeling for bio-imaging.

Purpose of the Study:

  • To induce blue fluorescence in graphene oxide (GO) suspensions.
  • To enable GO to function as both a cellular imaging and drug delivery agent.
  • To develop a simple, controllable method for enhancing GO's fluorescence for biomedical applications.

Main Methods:

  • A mild thermal annealing procedure was used to induce blue fluorescence in GO suspensions.
  • The procedure preserved oxygen functional groups on the graphene plane.
  • Conjugation of cancer drugs to GO was performed without significant cytotoxicity.

Main Results:

  • Blue fluorescence was successfully induced in GO suspensions via thermal annealing.
  • The functional groups on GO remained intact, allowing for drug conjugation.
  • GO demonstrated dual functionality as a cellular imaging and drug delivery agent in CT26 cancer cells.
  • No additional fluorescent protein labeling was required for imaging.

Conclusions:

  • Mild thermal annealing is an effective strategy to induce and tune the fluorescence of GO.
  • GO can serve as a dual-purpose agent for cancer cell imaging and drug delivery.
  • This approach offers a promising, label-free strategy for biomedical applications of GO.