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AUTHORS: Robert H. Demling, M.D. Leslie DeSanti R.N. Dennis P. Orgill, M.D. Ph.D.

(STRUCTURE, PROPERTIES AND EVIDENCED BASED CLINICAL EXPERIENCE IN BURNS)

 

A) OVERVIEW

STRUCTURE:

  • a biosynthetic skin substitute first developed in 1979 and since modified which is constructed of an outer silicone film 
    (the epidermal analog).
  • with a nylon fabric partially imbedded into the film
  • collagen (porcine type 1) is incorporated in both silicone and nylon components by being chemically cross-linked
  • the collagen peptides on the nylon bind to the wound surface fibrin and collagen resulting in the initial adherence 
    (dermal analog)
  • small pores are present in the structure to allow for drainage of exudate and also provide permeability 
    to topical antibiotics

Properties:

  • adherent to clean viable wound surface
  • impermeable to bacteria
  • controls evaporative water loss
  • flexible, durable, non-allergenic
  • permeable to topical antibiotics
  • stored room temperature
  • shelf-life of at least 3 years

Clinical Indications:

  • superficial to mid-partial thickness burns (once debrided of nonviable tissue)
  • excised burn wound with or without meshed autografts (need viable bed)
  • donor sites
  • partial thickness skin slough disorders

 


Biobrane Bilayer Structure is shown. Silicone outer layer acts like a protective epidermal barrier. The inner surface is composed of a three - dimensional interwoven nylon filament upon which collagen peptides are bonded. Initial wound adherence is the result of bonding of membrane collagen to surface fibrin. The second phase of adherence results from epidermal cells proliferating between the nylon matrix.

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Biobrane bilayer structure is shown


BIOBRANE STRUCTURE AND PROPERTIES

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Outer surface shown. NOTE: Presence of Pores


Biobrane on modest stretch: surface smooth

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Biobrane draped over skin demonstrating transparency


mono_threads_1.jpg (11938 bytes)

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Trifilament threads bonded with collagen exposed to wound (Biobrane)


mono_threads.jpg (16084 bytes)

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Monofilament threads bonded with collagen peptide (Biobrane L)


B) ASSESSMENT OF THE TEMPORARY SKIN SUBSTITUTE PROPERTIES OF BIOBRANE

 

Properties:

  • firm adherence to wound
  • barrier to evaporative water loss (maintains surface fluid layer)
  • avoids desiccation
  • barrier to bacteria
  • optimize healing environment
  • decreases pain
  • decrease wound exudate
  • durable, flexible, non-toxic
  • permeability to topical antibiotics

Adherence:

Biobrane contains a nylon fabric that is woven from tri-filament threads and covalently bonded with collagen peptides. The multiple filaments provide a high exposure to the wound surface resulting in an increasing adherence to the wound surface of partial thickness burn.

Biobrane L contains a nylon fabric woven from monofilament threads that provide a less dense matrix and less adherence, preferred e.g. on a donor site.

Adherence is biphasic: the initial adherence phase is due to fibrin-collagen (nylon) bonding and the second is the ingrowth of epithelial cells and fibrin between the threads. Adherence initially is comparable to allograft but biobrane adherence exceeds allograft by 3-5 days. For comparisons of adherence between skin substitutes see Section IV.

 

Water Vapor Transport

A decrease in water vapor transport is essential to avoid wound desiccation. However, some water vapor permeability is beneficial in preventing excess fluid accumulation.

Biobrane is nearly as effective as normal skin as a water vapor barrier after day 5 
(Tavis et al. A new composite skin prosthesis. Burn 1978: 7; 1283.


Barrier to Bacteria

Assessment performed by surface cultures of wounds excised and covered with biobrane, allograft or treated open.

In this study Biobrane was more effective than allograft as a bacterial barrier Tavis et al. 
A new composite skin prosthesis. Burns 1978: 7; 1233.

  • Optimizing healing environment

(comparative studies in section E demonstrate biobrane to increase re-epithelialization rate compared to topical antibiotics or exeroform gauze

  • Decrease pain

(comparative studies in section E demonstrate biobrane to decrease pain compared to topical antibiotics or xeroform gauze

  • Decrease wound exudate

(comparative studies demonstrate biobrane to decrease exudate compared to fine mesh gauze

  • Durability, flexibility

a minimal elongation of 350± 50% and a burst strength of 10.3± 2 lb/inch have been reported (Tavis, et al)

Permeability to antibiotics

Permeability to 1% silver Sulfadiazine comparing biobrane without pores to the standard with pores. The standard biobrane is very permeable to topical antibiotics. (Tavis et.al.)

  • Safety

- the value for the primary skin irritation index falls within the "non-irritant" category

- intracutaneous toxicity studies were reportedly negative

- pyrogenicity studies were reported negative


 

C) MECHANISM OF ACTION

The mechanism of action is initially described using schemas to be followed by clinical application.

 

Biobrane bilayer structure is shown. The silicone outer layer acts like a protective epidermal barrier. The inner surface composed of a three dimensional interwoven nylon filament structure upon which collagen peptides are boarded. Initial wound adherence is the result of bonding of the inner membrane collagen coated nylon to surface fibrin. The second phase of increasing adherence results from epidermal cells migrating and proliferating between the nylon matrix.

 

A superficial partial thickness burn is shown. The zone of necrosis is confined to the upper (papillary) dermis and is usually separated by a layer of edema from the viable wound surface. Note the zone of injury which needs to be protected.

 

Superficial burn debrided to viable wound bed. Note surface fibrin and collagen. Also note increased proteolytic activity which is not suppressed by immediate wound closure, will produce increased injury.

 

Bilayer biobrane ready to be placed on clean wound. Note outer silicone layer (epidermal analog) and inner nylon mesh coated with collagen to adhere to surface (dermal analog)

 

Biobrane in place, adhered to surface by nylon-collagen mesh. Note preservation of thin water layer on surface to allow epithelial migration along inner layer.

 

Biobrane peeled back from surface to demonstrate rapid migration of new epithelium along nylon-collagen mesh. As epithelialization increases the biobrane becomes more opaque. The minimal exudate produced, drains out the pores.

 

Biobrane removed with re-epithelialization.

 

 

 

 

 


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