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    Prajakta.S. Kolhatkar& Avanti Kulkarni

    FROMJAWAHARLAL DARDA INSTITUTE OF

    ENGG.& TECHNOLOGY

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    Technoxtreme-09

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    INTRODUCTION

    During the last two decades many significant

    advances have been made in development of

    biocompatible materials for biomedical

    applications and industrial applications also. Inbiomedical field the aim is to develop and

    characterize artificial materials for use in human

    body to measure, restore and improve

    physiological function and enhance survival and

    quality of life.

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    Biopolymer properties

    o Non-toxic (biosafe): Non- pyrogenic, Non-

    hemolytic, Chronically, non- inflammative,

    o Effective: Functionality, Performance, Durability,

    etc

    o Sterilizable: Ethylene oxide, c-Irradiation, Electron

    beams, Autoclave, Dry heating,etc.

    o Biocompatible: Interfacially, Mechanically, andBiologically

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    VARIOUS MEDICAL APPLICATIONS

    Suturing

    Fixation

    Adhesion

    Covering

    Occlusion

    Isolation

    Contact inhibition

    Controlled drug delivery

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    Biocompatible polymers used

    Biocompatible polymers include any synthetic or

    Natural polymers,metals,alloys,glasses, ceramics,

    composites, or other nonviable substances including

    tissue rendered nonviable. Recently the termBiocompatible polymers (biomaterial) was defined as

    a nonviable material used in medical device

    applications that is intended to interact with a

    biological system. In the other word, it can bedefined as materials that are used in contact with

    tissue, blood, cells, protein and any other living

    substance

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    Biocompatible polymers in general are used

    To replace tissues which are diseased or otherwisenonfunctional, as in joint replacements, artificial heartvalves and arteries, tooth reconstruction and intraocularlenses;

    To assist in the repair of tissue, including the obvioussutures but also bone fracture plates, ligament andtendon repair devices;

    To replace all or part of the function of the major organs,such as in haemodialysisoxygenation (lungs), left

    ventricular or whole heart assistance (heart), perfusion(liver), and insulin delivery (pancreas);

    To deliver drugs to the body, either to targeted sites (e.g.directly to a tumour) orsustained delivery rates (insulin,pilocarpin and contraceptives).

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    BIOCOMPATIBLE POLYMERS IN DRUG

    DELIVERY SYSTEM

    The goal of the controlled release devices is to

    maintain the drug in the desired therapeutic

    range with just a single dose. Localized

    delivery of the drug to a particular body

    compartment lowers the systemic drug level,

    reduces the need for follow-up care, preserves

    medications that are rapidly destroyed by thebody, and increases patient comfort and/or

    improves compliance.

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    Collagen-Based Localized Drug

    Delivery Systems

    Biodegradable polymers make ideal vehicles for

    localized drug delivery. Systems based upon synthetic

    polymers are currently under development.

    However, collagen offers the advantages of a naturaland well-established biocompatible material,

    together with its complimentary wound healing and

    haemostatic properties. Some companies pioneered

    the use of collagen for localized drug delivery withthe breakthrough therapeutic product Collatamp G,

    based upon its CollaRx platform

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    Collarx technology

    Collarx is a localized drug delivery system basedupon a type-1 collagen matrix derived from bovine or

    equine Achilles tendon. Products may be formatted

    either as a lyophilized porous sponge or as a

    transparent/translucent sheet (or membrane)

    about 50 m in thickness (Figure 2

    In vivo, drug is released by a combination of

    diffusion and natural enzymatic breakdown of thecollagen matrix. This provides both rapid and

    prolonged release. The matrix itself is fully resorbed

    within one to seven weeks according to implant

    location .

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    Lyophilized porous sponge

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    Transparent Sheet

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    Collatamp G Collatamp G is an implantable type-I collagen sponge

    impregnated with 2.0 mg/cm2 of gentamicin sulfate.

    It is approved as a medicinal drug product in many

    European countries and is currently marketed under

    various brand names by Schering PloughCorporation. The product is indicated for the surgical

    treatment and post-surgical prevention of infection

    in bone and soft tissue and has been clinically proven

    to reduce rates of infection and substantially reducethe average duration of hospital stay.

    Pharmacokinetic studies have demonstrated that

    high local concentrations of gentamicin.

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    Lactide and Glycolide

    The incidence of mycobacterial infections has

    increased rapidly in recent years; one-third of the

    world's population is infected with Mycobacterium

    tuberculosis, the causative agent of tuberculosis (TB).

    Chemotherapy of tuberculosis is complicated by theneed for multi-drug regimens given over long

    periods. Current short-course chemotherapy (SCC)

    involves daily administration of isoniazid (INH),

    rifampicin (RIF) and pyrazinamide (PZA) for a periodof 69 months. Therapy for TB may be further

    complicated by patient non-compliance and the

    development of multi-drug resistant (MDR) strains.

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    Lactide and Glycolide

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    ADVANCED DELIVERY DEVICES

    Recently biocompatible biopolymers are used for cell-

    based therapies delivered via devices.These proceduresuse human or animal ells to produce naturally occurring

    proteins for administration to patients to treat symptoms

    or cure disease. Under this section devices that are being

    developed to deliver large molecular weight proteins likeinsulin through routes other than conventional

    injection.In delivery of insulin the drug (insulin) is being

    manufactured not in the drug companys facilities, but in

    the transplanted cell, and delivered directly to thepatient in response to glucose levels in his/her

    bloodstream.

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    BIOCOMPATIBLE POLYMERS IN

    BONE GRAFTING Periprosthetic osteolysis bone loss in the vicinity of a

    prosthesisis the most serious problem limiting the longevity

    of artificial joints. It is caused by bone-resorptive responsesto wear particles originating from the articulating surface.

    Mechanical studies using a hip-joint simulator revealed that

    the MPC grafting a hip-joint simulator revealed that the MPC

    grafting Osteoclastic bone resorption induced by

    subperiosteal injection of particles onto mouse calvariae was

    abolished by the MPC grafting on particles

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    CONCLUSION

    Textile materials like biocompatible polymers

    continue to serve an important function in the

    development of a range of medical and

    surgical products. The introduction of newmaterials, the improvement in production

    techniques and fiber properties, and the use

    of more accurate and comprehensive testinghave all had significant influence on advancing

    fibers for medical applications.