interpenetrating networks for delivery systems client: professor w. john kao, school of pharmacy...

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Interpenetrating Networks for Delivery Systems Client: Professor W. John Kao, School of Pharmacy & Department of Biomedical Engineering Advisor: Professor Naomi Chesler, Department of Biomedical Engineering Ashley Huth Claire Flanagan Adam Rieves Jon Sass

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Interpenetrating Networks for Delivery Systems

Client: Professor W. John Kao, School of Pharmacy & Department of Biomedical Engineering

Advisor: Professor Naomi Chesler, Department of Biomedical Engineering

Ashley HuthClaire FlanaganAdam Rieves

Jon Sass

Overview• Background Information

• Interpenetrating Networks (IPNs)• Competing Products• Past Semester

• Problem Statement• Design Requirements• Proposed Designs• Future Work• Questions

Problem Statement• To design a novel delivery mechanism

to reconstitute the components of an interpenetrating network (IPN).

Background: IPNs

*Kao, W.J.

What is an IPN?A bioactive wound dressing for

large surface area wounds

IPNConventional Dressings

Irregular Wound

Background: IPNs

• Kao, W.J.

Solution(drugs + matrix component)

Covalently Linked Therapeutic(s) and/orCell Adhesion Ligands

Soluble Therapeutic(s)

Biodegradable Gelatin Backbone

PEG-diacrylate(2-3.4 kDa )

in situ UV curing

IPNs are composed of multiple components

Clinical Application• Benefits

– Biocompatible– Moist healing environment– Conforms to irregular wounds– Covers large surface area wounds– Delivers drug cocktails

• Issues– Heat– Uneven administration– Lengthy application process

Current Administration Technique

Ingredients/drug(s) in singlecontainer

Mix11

Cover55

Heat22

33 Inject Syringe is use to administer solution

44 Curein 30 sec to obtain a rubbery film

66 Sustained Releasewhile the IPN biodegrades

Day7

Day3Day

1

77 Clean

*Kao, W.J

Components•pegDA•Gelatin•Photoinitator•Water

Last Semester• Focused on optimizing IPN solution

composition– Gelatin dissolution impacts efficacy & administration of IPNs

– Integrated laboratory & design-based research

• Developed IPN recipe

• Modified IPN administration

This Semester• Administration technique

• Product packaging

• Further laboratory research

Design Requirements• Minimal preparation and effort required to

administer the IPN• Compartmentalization • Even spray pattern• Uniform solution• Straightforward mixing procedure• Disposable • Can be sterilized • Low-cost• Few parts

Competing Products

• Duoject Medical Systems Inc. – Inter-Vial

• Debiotech – Clip’n’ject

• U-Mix – Travel Bottle

• Hansplast – Spray Bandage

Design 1: Syringe

• Liquid in plunger• Powder stored in

barrel• Mechanism to release

liquid into powder• Hand mixing• Hand powered

delivery• Luer-Lock spray tip

Design 1: Syringe• Pros

– All in one packaging– Easy application– Controllable spray rate

• Cons– Custom manufacturing required– Moving parts

Design 2: Pressurized Bottle

• Manual pressure vacuum

• Unique cap design– Facilitates stirring

mechanism

• Perforated seal

Design 3: Pressurized Bottle• Pros

– Incorporates mixing mechanism– Provides slow release of photo-initiator

• Cons– Laborious application technique– Non-standard parts

Design 1: Spray Bottle

• Threaded straw • Blades puncture inner

container• Single pump, single

spray• Includes mixing

mechanism

Design 3: Spray Bottle• Pros

– Incorporates mixing mechanism– Provides slow release of photo-initiator

• Cons– Laborious application technique– Non-standard parts

Design Matrix

Criteria WeightDesign 1 Syringe

Design 2 Pressurize

Design 3 Spray

Mixing Procedure 15 10 9 12Uniform Solution 10 6 7 7Compartmentalization 10 9 5 8Parts Availability 10 7 9 6Application Ergonomics 10 8 6 4Safety 10 8 6 8Cost 10 5 3 7Sterility 5 5 3 4Scalability 5 5 2 4Spray Pattern 5 4 5 2Client Preference 5 5 5 3Photo-initiator Protection 5 3 5 4TOTAL 100 75 65 69

Future Work• Test cold-water soluble gelatin

• Develop-Manufacture-Test prototype

• Research photoinitiators

• Continue patent search