Medical Polymers :
Emerging Trends & Opportunities
Polymers/Biopolymers For Modern
Wound Dressing
Wound dressing has remained challenging for some life
threatening wounds such as Burning.
Wound dressing has remained challenging for some
life-threatening wounds such as burning. Researchers
have been engaged in looking for better solutions. A
review paper given in the “Journal of Material
Sciences & Engineering” ( web link for detailed paper
Future Needs for Would Dressings)
Despite the various methods and materials for wound
dressings, to date, no wound dressing fully satisfies
the requirements of an ideal substitute for skin ECM (Extracellular
Matrix ). Most wound dressings are limited by fast
degradation, weak adhesiveness and absorption, lack of
drug release properties, poor oxygen permeability, as
well as not being able to prevent protein adhesion
onto the wound dressing surface. It is urgent to
design and fabricate wound dressings which can
address these problems simultaneously, thereby leading
to improved wound management, creating an easy
solution for wounds, and decreasing death rate induced
by severe wounds and bleeding.
Modern Wound Dressing Materials
Synthetic polymers such as polyvinyldene floride (PVDF)
and polypropylene (PP) have been widely used for wound
dressing materials. Poly (ε-caprolactone) (PCL),
polyethylene glycol (PEG), polyethylene oxide (PEO),
polyurethane (PU), poly (vinyl alcohol) (PVA), poly
(lactic acid) (PLA), and poly (lactic-co-glycolic
acid) (PLGA) are frequently used synthetic materials
that have been approved by Food and Drug
Administration (FDA) for biomedical applications, due
to their good biocompatibility, biodegradability and
non-toxic properties. For example, PLGA is
commercially available, inexpensive, biocompatible,
biodegradable, and showed sustained drug release
properties, making it the ideal candidate for drug
delivery and other biomedical applications. Moreover,
Porporato discovered that lactate played an important
role in promoting angiogenesis and wound healing
process, and concluded that PLGA to be the most
suitable polymer to provide lactate for enhanced wound
management. PEG displays excellent biocompatibility,
biodegradability, hydrophilicity and wettability. It
is inexpensive and readily available, and therefore
widely used for biomedical applications. More
recently, Kim has shown that PEG provides antifouling
properties, preventing the adsorption of protein and
other biomolecules on to nanofiber surface, which
enhances drug release properties and aids in
maintenance of nanofiber surface properties during
use. Hydrogels and nanofibrous scaffolds based on
these synthetic polymers have been fabricated for
biomedical applications with good mechanical
properties.
However, the application of these synthetic polymers
alone as wound dressings are limited by their adhesive
properties and their ability to accelerate wound
healing process.
Therefore, it is critical to produce a new and
improved wound dressing by synthesizing, modifying,
and systematically designing wound dressing materials
with good mechanical properties while accelerating the
healing process at molecular, cellular and systematic
levels. It is also desirable for wound dressings to
have good drug release properties to further promote
the wound healing process. Detailed research article
is given at the following web link.
Polymeric Biomaterials For 3D
Printing In Medicine
Although much progress has been made with 3D printing
technology, there are still remarkable issues to
overcome (such as standardization and integration of
an entire biofabrication platform, software design,
capabilities of the 3D printers, reproducibility,
quality by design, biomaterials characterization, and
regulatory hurdles) before it can be recognized as a
conventional biofabrication technique in medicine and
reach the medical market. Among these issues, the
major bottleneck is the lack of heterogeneity
biomaterials allowing their reliable clinical use.
Generally, printable materials as polymers, hydrogels,
or bioinks must: (1) have adequate viscosity that
allows being printable and structurally stable, (2)
have the capability to form 3D structure within a few
minutes, (3) have the possibility of being
mechanically reinforced through UV irradiation,
biological (e.g. transglutaminase, sortase, tyrosinase,
lysil-amine oxidase), or chemical (e.g. Michael-type
addition, thiolene reaction, orthogonal reaction)
cross-linking, (4) have tunable mechanical properties,
(5) be biocompatible, (6) have adequate degradation
kinetics, (7) form nontoxic degradation by product s ,
( 8 ) be biomimetic, and (9) be able to control
release molecules or drugs. In addition, biomaterial
inks should be easily manufactured and processed,
affordable, and commercially available.
In this context, 3D printing can transform healthcare
through personalized medicine, thus improving patient
compliance by tailoring the medication to the patient.
This can be achieved through on-demand manufacturing
in clinical settings to offer the best medical care.
3D printable materials Solid polymers-based inks
Polymers are the most common types of biomaterials
used in 3D printing technologies [57, 58], since they
come in the form of filaments for fused deposition
modeling (FDM), powder-beads for selective laser
sintering (SLS), solutions for stereolithography (SLA),
and gels for direct ink writing (DIW) (Fig. 2).
Further, they are biocompatible, have tunable
mechanical properties, degradation rates, and can be
dissolved in rapidly evaporating organic solvents such
as dichloromethane, tetrahydrofuran or dimethyl
sulfoxide.
Fig. . Schematic representation of 3D printing
techniques. (a) Fused deposition modeling (FDM), (b)
stereolithography (SLA), (c) selective laser sintering
(SLS), and (d) direct ink writing (DIW). Table 1.
Common polymers used in 3D printing and their
properties
Polymers used in 3D printing technologies come in
the form of filaments for fused deposition modeling (FDM),
powder-beads for selective laser sintering (SLS),
solutions for stereolithography (SLA), and gels for
direct ink writing (DIW). |