Next Article in Journal
Editorial on the Special Issue “Novel Methods of Diagnostics of Thyroid and Parathyroid Lesions”
Next Article in Special Issue
An Innovative Minimally Invasive Oncoplastic Technique for Early Breast Cancer: The Spoon-Shape Technique
Previous Article in Journal
Efficacy and Safety of Rituximab in Autoimmune Disease—Associated Interstitial Lung Disease: A Prospective Cohort Study
Previous Article in Special Issue
Should Ultrasound-Guided High Frequency Focused Ultrasound Be Considered as an Alternative Non-Surgical Treatment of Uterine Fibroids in Non-Asiatic Countries? An Opinion Paper
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JCM
Volume 11
Issue 4
10.3390/jcm11040931
jcm-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Chemically Modified Hyaluronic Acid for Prevention of Post-Surgical Adhesions: New Aspects of Gel Barriers Physical Profiles

by
Luz Angela Torres-de la Roche
1,*,
Véronique Bérard
2,
Maya Sophie de Wilde
1,
Rajesh Devassy
1,
Markus Wallwiener
3 and
Rudy Leon De Wilde
1
1
University Hospital for Gynecology, Pius Hospital, University Medicine Oldenburg, 26121 Oldenburg, Germany
2
Laboratoire Interdisciplinaire Carnot de Bourgogne, UFR des Sciences de Santé, 21000 Dijon, France
3
University Hospital for Obstetrics and Gynecology, University Medicine Heidelberg, 69120 Heidelberg, Germany
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2022, 11(4), 931; https://doi.org/10.3390/jcm11040931
Submission received: 30 November 2021 / Revised: 27 January 2022 / Accepted: 8 February 2022 / Published: 11 February 2022
(This article belongs to the Special Issue Challenges and Controversies in Minimally Invasive Surgery: What Is Really New in Gynecologic Surgery?)
Browse Figures
Versions Notes

Abstract

:
This study was conducted to provide information regarding the chemistry—including structure, synthesis, formulation, and mechanical properties—of two types of chemically modified anti-adhesion gels made of hyaluronic acid. Gel A (Hyalobarrier®) and gels B and C (HyaRegen® and MetaRegen®) that are used in postsurgical adhesion prevention. To date, little information is available on their physicochemical attributes. This information is necessary in order to understand the differences in their in vivo behavior. Methods: Comparative analyses were conducted under laboratory-controlled conditions, including measuring the shear viscosity, storage modulus G’, peel strength, and extrusion forces. Results: All polymers exhibited viscoelastic behavior. Polymer A showed a shear viscosity approximately three times larger than both polymers B and C (114 Pa.s−1 vs. 36–38 Pa.s−1) over the shear-rate range measured, indicating a possible better ability to resist flows and potentially remain in place at the site of application in vivo. The results of storage modulus (G’) measurements showed 100 Pa for polymer A and 16 Pa and 20 Pa for polymers B and C, respectively. This translated into a weaker elastic behavior for gels B and C, and a lower ability to resist sudden deformation. The peel test results showed a rupture strength of 72 mN (0.016 lbf) for polymer A, 39.6 mN (0.0089 lbf) for polymer B, and 38.3 mN (0.0086 lbf) for polymers C, indicating possible higher adhesive properties for polymer A. Tests measuring the extrudability of the hyaluronic acid gels in their commercial syringes showed an average extrusion force of 20 N (4.5 lbf) for polymer A, 28 N (6.33 lbf) for polymer B, and 17 N (3.79 lbf) for polymer C. Conclusions: Modified anti-adhesion gels made of hyaluronic acid differed in mechanical properties and concentration. Further clinical studies are needed to confirm whether these differences make one polymer easier to apply during surgery and more likely to stay in place longer after in vivo application, and to determine which is potentially superior in terms of preventing adhesions.

1. Introduction

Adhesions are defined as internal scar tissue that may form as part of the body’s healing process after surgery [1]. They constitute a widespread complication of abdominopelvic surgery, developing in 79–90% of patients who receive open abdominal, pelvic, or hysteroscopy surgery [2,3,4]. Adhesions may cause acute abdominal complications such as bowel obstruction, chronic pelvic pain, female infertility, or some combination of the above, and patients may require reoperation [1,5,6,7,8,9,10]. The formation of the fibrous scar tissue responsible for adhesions is at least partly the result of ischemia and inflammation secondary to perioperative trauma [11], and the critical period in which adhesions appear is the first three to five postoperative days [12].
In the ten years following open surgery, one study documented that approximately one in three patients were readmitted to the hospital for causes possibly related to adhesions, and 5.7% of patients were readmitted for causes directly related to adhesions [13]. Even after the widespread adoption of laparoscopic surgery, and although the incidence of hospital readmissions related to adhesions has been reduced, adhesion-related morbidity remains significant. One in six patients treated laparoscopically are readmitted for a complication possibly related to adhesion, and 1.7% for a complication directly related to adhesion [13].
Although primary prevention based on meticulous surgical techniques to limit ischemic factors and peritoneal inflammation appears to be the best treatment strategy [10], it is not sufficient to prevent postoperative adhesions [2,3,4]. Therefore, the interest in secondary prevention using physical adhesion barriers is growing. The underlying principle here is based on interposing a physical barrier that prevents damaged peritoneal surfaces from making contact until the peritoneum heals [4,5]. At present, such adhesion barriers are rarely used in daily practice, despite existing evidence showing their efficacy in reducing adhesion formation [14,15], and the existence of a large offer of natural and synthetic biomaterials (hyaluronan, alginate, cellulose, starch, polyethylene glycol, etc.) available in different forms (gel, film, sprayable powder, sponge, liquid, etc.) [16,17].
Hyaluronic acid (HA) is a natural polymer extensively used in biomedical applications due to its excellent biocompatibility, swelling properties, and tunable mechanical properties [18]. HA is a macromolecule of high molecular weight (100,000 to 6 million Daltons) that belongs to the glycosaminoglycan family. Its structure is composed of two sugar-based moieties (N-acetylglucosamine and D-glucuronic acid), which combine to form a repeating disaccharide polymer [19,20] linked via alternating β-1,4 and β-1,3 glycosidic bonds (Figure 1). Derivatives of hyaluronic acid form the basis of a number of anti-adhesion gels [1].
Many physical and chemical properties underlie the physiological and pharmacological characteristics of HA. It is highly hydrophilic, retaining or combining with water to form a tissue-moisturizing complex. From a rheological perspective, HA exhibits viscoelastic and shear thinning properties, thereby cushioning and lubricating skeletal structures. Finally, it has been demonstrated to have antioxidant properties due to its free-radical-scavenging activity [19,20]. HA has been shown to bind to specific receptors on the surface of certain cells involved in cellular adhesion and mobility as well as in inflammatory processes [20,21]. It also interacts with extracellular proteins, binding to collagen during healing and to fibrin during the inflammatory phase [20]. Moreover, HA has the advantage of being of physiological origin, biocompatible, nonallergenic, noninflammatory, and biodegradable [22,23,24]. Hyaluronan is a major component of many body tissues and fluids, where it plays a role in physical support and mechanical protection [25]. Finally, HA has been being utilized to prevent surgical adhesions for over 10 years [26], and its efficacy has been confirmed on several occasions, including recently in a meta-analysis [27]. Different formulations of HA are available for adhesion-prevention therapy.
The aim of this work was to directly compare two types of HA-derived adhesion barriers featuring different reticulation: the established auto-crosslinked Hyalobarrier® gel (Anika Therapeutics) with a zero-length crosslinking, and the more recent crosslinked HyaRegen® and MateRegen® gels (BioRegen) with a chemically modified longer crosslink. In this laboratory test we evaluate how these two types of polymers differ in their chemistry, formulation, and mechanical properties.

2. Materials and Methods

The analysis was conducted under laboratory-controlled conditions on the HA-based products described in Table 1. The following aspects were investigated: chemistry, formulation, and mechanical properties.
The flow properties of the different compounds were analyzed, assessing steady-shear viscosity and storage modulus using a TA Instruments rheometers, model DHR-1 and AR-1500ex. We employed the a cone–plate geometry for the analysis (hard anodized aluminum, ST, 40 m, 2°, Smart Swap, TA Instruments, New Castle, DE, USA). To determine steady-shear viscosity, a rotational rheometer, TA Instruments AR-1500ex, with a 60 mm, 1° cone at 20 °C, was used. The viscosity response was observed at a shear rate of 1.0 s−1. For storage modulus (G’), that is, the elastic component, the small-angle oscillatory shear test was used, measuring the elasticity over a range of frequencies. The more rapidly the material is deformed, the stronger the elastic effects are, and the higher the frequency, the more rapid the deformation. Typically, G’ increases with frequency.
A peel test was conducted on both types of anti-adhesion gel to determine their adhesive strength to a hydrophilic surface, simulating human tissue. The hydrophilic surface was created by wetting paper strips. The gels were applied to the paper using a glass mold to give a uniform coating of 21 mm × 75 mm × 1 mm in size. The piece of paper was applied to the top of the gel. The sample was then placed in a tensile tester and the force measured as the strips were pulled apart at a rate of 330 mm/min until the materials separated, corresponding to the rupture strength. Experiments were performed at room temperature on a MARK-10 instrument, Motorized Test Stand ESM301L model (Mark-10 Corporation, Copiague, NY, USA)
Extrusion force tests were performed on both types of gels to determine their extrudability (i.e., the force required to push the gel out of the cannula), using the same MARK-10 instrument with the force sensor traveling downwards in a compression mode. Extrusion force tests were performed on all three gels using a 5 cm cannula with an inside diameter of 2.0 mm, at a linear rate of 12 mm/min, at room temperature. During the test, the gel was compressed until it flowed out of the cannula, corresponding to the extrusion force. In this case, the gels were not transferred into the same-sized syringe, but rather the test was performed using syringes from the original product. Thus, the extrusion force comparison reflected the actual usage.

3. Results

3.1. Chemical Structure

The HA-based products are described in Table 1, and their chemical structures are depicted in Figure 1. In the auto-crosslinked polymer A, the HA chains are linked by an ester function, formed by a condensation reaction (displacement of a water molecule) between the free primary hydroxyl function and the carboxylic acid residue of the HA chains. This is often referred to as a ‘zero-length’ crosslink, as no foreign moiety is introduced into the material. The final product is a reticulated form of HA in a gel form that has only been chemically modified to a minimal degree. The hydrolysis of the ester functional groups reversibly regenerates unmodified HA.
The crosslinked polymer (products B and C) is a chemically modified, reticulated polymer of HA, crosslinked by a long chain between the carboxylic acid functional groups of the HA chains, containing two hydrazide functional groups and a disulfide bridge in the center (Figure 1).

3.2. Formulation and Material Properties

The main evaluated physical properties of both types of polymers are summarized in Table 2. According to the manufacturer specifications, the two types of gels have different HA concentrations, with gel A being approximately six times more concentrated than gel B (30 mg/mL vs. 5 mg/mL). To demonstrate the ability of the polymers to resist flow and remain in place at the site of application, steady-shear viscosity tests were performed on each gel. The test results in the comparative flow curves show that the steady-shear viscosity of all polymers decreased with flow rate, demonstrating viscoelastic behavior. The results also show that polymer A had a shear viscosity approximately three times as large as polymers B and C (114 Pa.s−1 vs. 36–38 Pa.s−1) over the shear-rate range measured. These differences in physical properties could be attributable to the different synthesis methods of the polymers being evaluated.
The formation of polymer A is depicted in Figure 2. The t-butyl-ammonium hyaluronate intermediate is formed from sodium hyaluronate via an ion-exchange step. This hydrophobic salt of HA is then dissolved in N-methyl-pyrrolidone (NMP), where the 2-chloro-1-methyl pyridinium iodide reagent is introduced to react with the carboxylic group of the glucuronic acid unit, forming an ‘active’ ester. The ester is displaced by the primary hydroxyl group on C-6 of N-acetylglucosamine of another chain or another part of the same chain, forming the ‘zero-length’ ester bond. The level of impurities in the resulting auto-crosslinked gel is controlled. The purity was assessed using two orthogonal methods, a colorimetric analysis by spectrometry and a chromatographic analysis by gel-permeation chromatographic HPLC. The presence of any potential process impurities was quantified to be less than 0.2% w/w.
Condensation reaction (displacement of a water molecule) yields an ester link between the HA chains. The crosslinked polymers B and C are chemically identical and produced according to the synthetic route shown in Figure 3. They are synthesized by chemically modified HA chains, linking the carboxylic acid groups of glucuronic acid moieties with hydrazides as a cross-link [28,29,30,31].
The process is as follows: HA is activated with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) under acidic conditions in aqueous media, forming an O-acylisourea side group on the HA chain. Then, dithiodipropionic dihydrazide (DTP) reacts with this modified HA, displacing the O-acylisourea and forming amides or hydrazides, which completes the reaction. The disulfide bond is reduced by dithiothreitol (DTT) to thiol groups, breaking the crosslink and generating thiolated HA. The solution is then clarified by centrifugation and the purity of the thiolated HA measured by gel-permeation chromatography (GPC) and 1H NMR. The thiolated material is subsequently loaded into syringes and whatever dissolved oxygen is present oxidizes some percentage of the thiol groups back to a disulfide bond, forming the final gel (Figure 3). The final purity level required for crosslinked gels B and C is not known, nor is any toxicological information available for either the dithiodipropionic acid esters (reaction intermediate) or the dithiodipropionic dihydrazide reagent.
The flow properties of modified HA gels were studied to demonstrate viscoelastic behavior by measuring steady-shear viscosity over a large range of shear rates. The results in Figure 4 show that all gels exhibited this behavior, highlighted by the flow curves that decrease with shear rate. It can also be observed that Hyalobarrier® had a shear viscosity approximately three times higher than HyaRegen® and MateRegen® throughout the range of shear rates studied.
To evaluate the elastic component, also called the storage modulus or G’, we compared all polymers by measuring G’ over a range of frequencies. The results (Figure 4a) showed that the dependence of G’ on frequency for products B and C was weak, and these polymers acted more like simple elastic solids. Hence, their resistance to a sudden deformation did not increase as it did for product A, which was higher at all measured frequencies. At low frequency (0.1 Hz), the resistance of product A was about four times greater, and at the higher frequency of 10 Hz, G’ was about ten times greater (Figure 4b).
To compare the adhesive strength between hyaluronan polymers, peel tests were conducted on all three gels under the same experimental conditions at a rate of 330 mm/min. The average forces measured are presented in Table 2 and illustrated in Figure 5. The results indicate that the rupture strength of polymer A (72.0 mN) was approximately two times higher than the rupture strengths of polymers B and C (39.6 and 38.3 mN, respectively).
Peel tests also revealed an interesting qualitative result. The photographs of the two peel strips after completing the peel strength test shown in Figure 6 indicate that polymer A adhered strongly to the strips and that the fracture occurred in the bulk of the material. There was a relatively even coating on both strips (Figure 6—Polymer A).
In the case of polymer B, peel strip photographs show large clumps and some bare patches without gel, indicating a weaker adherence to the hydrophilic paper surface (Figure 6—Polymer B). This indicates that the inherent gel particle size of gel B was larger and that the coating was not as uniform as that of gel A.
No difference was observed between the peel strength test results of polymers B and C (Figure 6).
The average extrusion forces were measured for all three polymers in their commercial syringes to better reflect actual product use. The average forces measured are presented in Table 2 and illustrated in Figure 7.
For polymer A, the measured force was 4.5 lbf (20 N). For polymer B, an extrusion force of 6.33 lbf (28 N) was observed, and a force of 3.79 lbf (17 N) was observed for polymer C. Due to the larger syringe diameter of gel B, it was expected to lead to an extrusion force greater than 6 lbf (27 N) (Table 2). The extrusion force on the 5 mL syringe of gel C was expected to be lower, given the low steady-shear viscosity observed for this crosslinked polymer, and this was borne out by the results.

4. Discussion

Despite the well-known effects of careful surgical technique in preventing the formation of adhesions [31], the burden of disease caused by postsurgical adhesions [13] has pushed the industry to produce safe and effective agents to minimize the damage that surgical trauma induces in peritoneal surfaces and organs [32,33]. Different products based on several chemically modified substances are now available. HA is currently one of the main compounds used in new products because it has anti-inflammatory properties and characteristics that play important roles in the wound healing process [34,35]. Furthermore, HA itself can serve as a barrier between tissues. Nevertheless, there are differences between products containing HA.
The anti-adhesive efficacy of the two types of HA-based products evaluated herein following gynecologic laparoscopic surgery has not yet been directly compared, although they were both demonstrated to be efficacious in prospective, randomized, placebo-controlled, observer-blinded studies [36,37,38,39,40]. Our analysis is the first one designed to determine the differences between these HA polymers with regard to their chemical structure and material properties in crosslinked (HyaRegen®/MateRegen®) and auto-crosslinked (Hyalobarrier®) anti-adhesion agents.
Regarding their chemical structure, both types of gel contain modified reticulated forms of HA. However, we observed a difference in the auto-crosslinked structure of polymer A, with no foreign moiety being introduced into the material. Under physiological conditions, gel A degrades by hydrolysis (addition of a water molecule), reforming the original, unmodified HA, and the polysaccharide backbone breaks down into carbon dioxide and water. Meanwhile, the HA chains of the crosslinked gels (B and C) are crosslinked by dihydrazide groups, with a new disulfide bridge in the center of the link. This is the result of hydrazine being used during synthesis. The hydrazide bond is quite stable, and it is likely that it remains intact and degrades only in vivo, while the HA chains themselves are substantially degraded. Further studies should explore foreign-body reactions during clinical use based on the structural differences of the two products. Whether the residual presence of hydrazine after the degradation of gels B and C could induce changes in hepatic function, as reported after prolonged high-dose exposure (8 h time-weighted average permissible exposure limit of 1 ppm or 1.3 mg/m3), should also be evaluated [41].
On the other hand, the flow properties of HA-based gels, and specially modified HA solutions, are complex. These systems exhibit viscoelastic behavior, often with a critical yield stress. These fluids are also ‘shear-thinning’ or pseudoplastic. The resistance to flow does not increase linearly with the flow rate: twice the flow rate requires less than twice the force. As viscosity represents the ratio of the driving force to the flow rate, steady-shear viscosity decreases with increasing flow rate. Gel A showed a shear viscosity approximately three times higher than those of gels B and C over the range of measured shear rates. This indicates that gel A is ‘thicker’, and therefore more likely to resist flow and remain in place at the application site in vivo.
Regarding the materials’ ability to store energy elastically, all gels were demonstrated to be viscoelastic. Elastic effects are usually measured by small-angle oscillatory shear tests, which characterize the ability of a material to deform rapidly in response to oscillatory shear applied at different frequencies. The higher the frequency, the faster the deformation, and the stronger the elastic effect. the measured dependence of G’ on frequency for products B and C was weaker. Their resistance to a sudden deformation did not increase with frequency as it did for product A. Indeed, the elastic modulus of gel A was higher at all measured frequencies, making this substance more likely to stay in place after application.
The rupture strength of polymer A was observed to be twice as high as polymers B and C, and photographs showed a weaker adherence to the hydrophilic paper surface for gels B and C, with larger gel particle sizes and less-uniform coatings.
It was not possible to draw preliminary conclusions about the high extrusion force measured on gel C with the 5 mL syringe. This requires further investigation of the yield stress properties of this polymer.

5. Conclusions

Auto-crosslinked polymer A and crosslinked polymers B and C are chemically modified HA gels used to prevent adhesions from developing after surgery. This first comparative study showed several chemical and mechanical differences between these types of polymers.
They differ in their chemical structure. Polymer A has a short, or ‘zero length’ cross-linking, resulting from a simple displacement of water molecules, with no foreign materials. Polymers B and C, on the other hand, present a longer cross-linking incorporating foreign fragments coming from the use of other chemical reagents during their synthesis, for which total hepatic innocuity remains to be demonstrated. They also differ in their concentration and mechanical properties, with gel A having a higher concentration of hyaluronic acid, a higher rupture strength, and higher viscoelastic properties than gels B and C.
While these initial results indicate that polymer A is more likely to resist flows and peeling than polymers B and C, further clinical studies directly comparing these gels are needed to confirm whether their physicochemical differences make one polymer easier to apply during surgery and more likely to stay in place longer after application in vivo, and to determine which is potentially superior in terms of adhesion prevention.

Author Contributions

L.A.T.-d.l.R.: conceptualization, funding acquisition, project administration. L.A.T.-d.l.R. and V.B., investigation and data curation. All authors: formal analysis. L.A.T.-d.l.R. and V.B.: writing—original draft. All authors: review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This study was partially sponsored by Nordic Pharma, Paris, France. RLDW-17.11.2020.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors thank Laurence Saya, Nordic Pharma, Paris, France, for her logistic support during the conduction of this study.

Conflicts of Interest

The authors declare that this study was conducted in the laboratory of Anika Therapeutics, USA/Nordic Pharma, France. Authors have received financial support to perform clinical studies by Nordic Pharma (MW, RLDW) or BioRegen Biomedical (Changzhou) Co., Ltd. (RLDW).

References

  1. Ahmad, G.; Thompson, M.; Kim, K.; Agarwal, P.; Mackie, F.L.; Dias, S.; Metwally, M.; Watson, A. Fluid and pharmacological agents for adhesion prevention after gynaecological surgery. Cochrane Database Syst. Rev. 2014, 7, CD001298. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Menzies, D.; Ellis, H. Intestinal obstruction from adhesions—How big is the problem? Ann. R. Coll. Surg. Engl. 1990, 72, 60–63. [Google Scholar] [PubMed]
  3. Stommel, M.W.; Ten Broek, R.P.; Strik, C.; Slooter, G.D.; Verhoef, C.; Grünhagen, D.J.; van Duijvendijk, P.; Bemelmans, M.H.; den Dulk, M.; Sietses, C.; et al. Multicenter observational study of adhesion formation after open- and laparoscopic surgery for colorectal cancer. Ann. Surg. 2018, 267, 743–748. [Google Scholar] [CrossRef]
  4. Diamond, M.P.; Freeman, M.L. Clinical implications of postsurgical adhesions. Hum. Reprod Update 2001, 7, 567–576. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Ten Broek, R.P.G.; Strik, C.; Issa, Y.; Bleichrodt, R.P.; van Goor, H. Adhesiolysis-related morbidity in abdominal surgery. Ann. Surg. 2013, 258, 98–106. [Google Scholar] [CrossRef] [PubMed]
  6. Ording Olsen, K.; Juul, S.; Berndtsson, I.; Oresland, T.; Laurberg, S. Ulcerative colitis: Female fecundity before diagnosis, during disease, and after surgery compared with a population sample. Gastroenterology 2002, 122, 15–19. [Google Scholar] [CrossRef]
  7. Parikh, J.A.; Ko, C.Y.; Maggard, M.A.; Zingmond, D.S. What is the rate of small bowel obstruction after colectomy? Am. Surg. 2008, 74, 1001–1005. [Google Scholar] [CrossRef]
  8. Leung, T.T.; Dixon, E.; Gill, M.; Mador, B.D.; Moulton, K.M.; Kaplan, G.G.; MacLean, A.R. Bowel obstruction following appendectomy: What is the true incidence? Ann. Surg. 2009, 250, 51–53. [Google Scholar] [CrossRef]
  9. De Wilde, R.L.; Trew, G.; Angioni, S.; Audebert, A.; Barri, P.; Chapron, C.; Cocci, M.E.; Degueldre, M.; DiZerega, G.; García, E.; et al. Postoperative abdominal adhesions and their prevention in gynaecological surgery. Expert consensus position. Gynecol. Surg. 2007, 4, 161–168. [Google Scholar] [CrossRef] [Green Version]
  10. Ait Menguellet, S.; Collinet, P.; Cosson, M.; Mariette, C.; Triboulet, J.P.; Vinatier, D. Interest in agents for adhesion prevention after gynecologic surgery. Gynecol. Obstet. Fertil. 2007, 35, 290–296. [Google Scholar] [CrossRef]
  11. Imai, A.; Suzuki, N. Topical non-barrier agents for postoperative adhesion prevention in animal models. Eur. J. Obstet. Gynecol. Reprod. Biol. 2010, 149, 131–135. [Google Scholar] [CrossRef] [PubMed]
  12. Koninckx, P.R.; Corona, R.; Timmerman, D.; Verguts, J.; Adamyan, L. Peritoneal full-conditioning reduces postoperative adhesions and pain: A randomised controlled trial in deep endometriosis surgery. J. Ovarian Res. 2013, 6, 90. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Krielen, P.; Stommel, M.W.; Pargmae, P.; Bouvy, N.D.; Bakkum, E.A.; Ellis, H.; Parker, M.C.; Griffiths, E.A.; van Goor, H.; Broek, R.P.G.T. Adhesion-related Readmissions After Open and Laparoscopic Surgery: A Retrospective Cohort Study (SCAR Update). Lancet 2020, 395, 33–41, Erratum in Lancet 2020, 395, 272. [Google Scholar] [CrossRef]
  14. Ten Broek, R.P.G.; Stommel, M.W.; Strik, C.; van Laarhoven, C.J.M.; Keus, F.; van Goor, H. Benefits and harms of adhesion barriers for abdominal surgery: A systematic review and meta-analysis. Lancet 2014, 383, 48–59. [Google Scholar] [CrossRef]
  15. van Steensel, S.; van den Hil, L.C.L.; Schreinemacher, M.H.F.; Ten Broek, R.P.G.; van Goor, H.; Bouvy, N.D. Adhesion awareness in 2016: An update of the national survey of surgeons. PLoS ONE 2018, 13, e0202418. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Park, H.; Baek, S.; Kang, H.; Lee, D. Biomaterials to Prevent Post-Operative Adhesion. Materials 2020, 13, 3056. [Google Scholar] [CrossRef] [PubMed]
  17. Chandel, A.K.S.; Shimizu, A.; Hasegawa, K.; Ito, T. Advancement of Biomaterial-Based Postoperative Adhesion Barriers. Macromol. Biosci. 2021, 21, e2000395. [Google Scholar] [CrossRef]
  18. Laurent, T.C.; Fraser, J.R.E. Hyaluronan. FASEB J. 1992, 6, 2397. [Google Scholar] [CrossRef]
  19. Meaume, S. Hyaluronic acid. Ann. Dermatol. Venereol. 2001, 47 (Suppl. S3–S4), 536–566. [Google Scholar]
  20. Bonnetblanc, J.M. Propriétés pharmacologiques de l’acide hyaluronique [Pharmacological properties of hyaluronic acid]. Ann. Dermatol. Venereol. 2001, S9–S12. (In French) [Google Scholar]
  21. Navsaria, H. L’acide hyaluronique, matériel biotechnologique [Pharmacological properties of hyaluronic acid]. Ann. Dermatol. Venereol. 2002, 129, 1227–1230. (In French) [Google Scholar] [PubMed]
  22. Nappi, C.; Di Spiezio Sardo, A.; Greco, E.; Guida, M.; Bettocchi, S.; Bifulco, G. Prevention of adhesions in gynaecological endoscopy. Hum. Reprod. Update 2007, 13, 379–394. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Mensitieri, M.; Ambrosio, L.; Nicolais, L.; Bellini, D.; O’Regan, M. Viscoelastic properties modulation of a novel autocrosslinked hyaluronic acid polymer. J. Mater. Sci. Mater. Med. 1996, 7, 695–698. [Google Scholar] [CrossRef]
  24. De Laco, P.A.; Stefanetti, M.; Pressato, D.; Piana, S.; Donà, M.; Pavesio, A.; Bovicelli, L. A novel hyaluronan-based gel in laparoscopic adhesion prevention: Preclinical evaluation in an animal model. Fertil. Steril. 1998, 69, 318–323. [Google Scholar] [CrossRef]
  25. Johns, B.D.; Keyport, G.M.; Hoehler, F.; DiZerega, G. Reduction of postsurgical adhesions with Intergel adhesion prevention solution: A multicenter study of safety and efficacy after conservative gynecologic surgery. Fertil. Steril. 2001, 76, 595–604. [Google Scholar] [CrossRef]
  26. Revaux, A.; Ducarme, G.; Luton, D. Prevention of intrauterine adhesions after hysteroscopic surgery. Gynecol. Obstet. Fertil. 2008, 36, 311–317. [Google Scholar] [CrossRef]
  27. Farag, S.; Padilla, P.F.; Smith, K.A.; Sprague, M.L.; Zimberg, S.E. Management, Prevention, and Sequelae of Adhesions in Women Undergoing Laparoscopic Gynecologic Surgery: A Systematic Review. Minim. Invasive Gynecol. 2018, 25, 1194–1216. [Google Scholar] [CrossRef]
  28. Shu, X.Z.; Liu, Y.; Luo, Y.; Roberts, M.C.; Prestwich, G.D. Disulfide cross-linked hyaluronan hydrogels. Biomacromelecules 2002, 3, 1304–1311. [Google Scholar] [CrossRef]
  29. Liu, Y.; Shu, X.Z.; Gray, S.D.; Prestwich, G.D. Disulfide-crosslinked hyaluronan–gelatin sponge: Growth of fibrous tissue in vivo. J. Biomed. Mater. Res. 2004, 68, 142–149. [Google Scholar] [CrossRef]
  30. Shu, X.Z.; Liu, Y.; Palumbo, F.S.; Luo, Y.; Prestwich, G.D. In situ crosslinkable hyaluronan hydrogels for tissue engineering. Biomaterials 2004, 25, 1339–1348. [Google Scholar]
  31. Shu, X.Z.; Liu, Y.; Palumbo, F.; Prestwich, G.D. Disulfide-crosslinked hyaluronan-gelatin hydrogel films: A covalent mimic of the extracellular matrix for in vitro cell growth. Biomaterials 2003, 24, 3825–3834. [Google Scholar] [CrossRef]
  32. Wallwiener, M.; Koninckx, P.R.; Hackethal, A.; Brölmann, H.; Lundorff, P.; Mara, M.; Wattiez, A.; De Wilde, R.L. A European survey on awareness of post-surgical adhesions among gynecological surgeons. Gynecol. Surg. 2014, 11, 105–112. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Torres-de la Roche, L.A.; Herrmann, A.; Cezar, C.; Larbig, A.; Leicher, L.; De Wilde, M.S.; De Wilde, R.L. Prophylaxis of peritoneal adhesions: Practical issues to consider when using antiadhesion agents. Int. J. Health Med. Sci 2017, 3, 1–5. [Google Scholar]
  34. Frenkel, J.S. The role of hyaluronan in wound healing. Int Wound J. 2014, 11, 159–163. [Google Scholar] [CrossRef] [PubMed]
  35. Neuman, M.G.; Nanau, R.M.; Oruña-Sanchez, L.; Coto, G. Hyaluronic Acid and Wound Healing. J. Pharm. Pharm. Sci 2015, 18, 53–60. [Google Scholar] [CrossRef] [Green Version]
  36. Guida, M.; Acunzo, G.; Di Spiezio Sardo, A.; Bifulco, G.; Piccoli, R.; Pellicano, M.; Cerrota, G.; Cirillo, D.; Nappi, C. Effectiveness of auto-crosslinked hyaluronic acid gel in the prevention of intrauterine adhesions after hysteroscopic surgery: A prospective, randomized, controlled study. Hum. Reprod. 2004, 19, 1461–1464. [Google Scholar] [CrossRef] [Green Version]
  37. Hooker, A.B.; de Leeuw, R.; van de Ven, P.M.; Bakkum, E.A.; Thurkow, A.L.; Vogel, N.E.A.; van Vliet, H.A.A.A.M.; Bongers, M.Y.; Emanuel, M.H.; Verdonkschot, A.E.M.; et al. Prevalence of intrauterine adhesions after the application of hyaluronic acid gel after dilatation and curettage in women with at least one previous curettage: Short-term outcomes of a multicenter, prospective randomized controlled trial. Fertil. Steril. 2017, 107, 1223–1231. [Google Scholar] [CrossRef] [Green Version]
  38. Liu, C.; Lu, Q.; Zhang, Z.; Xue, M.; Zhang, Y.; Zhang, Y.; Wang, H.; Li, H.; Zhou, Y.; Zhang, Z.; et al. A Randomized Controlled Trial on the Efficacy and Safety of a New Crosslinked Hyaluronan Gel in Reducing Adhesions after Gynecologic Laparoscopic Surgeries. J. Minim. Invasive Gynecol. 2015, 22, 853–863. [Google Scholar] [CrossRef]
  39. Li, X.; Wu, L.; Zhou, Y.; Fan, X.; Huang, J.; Wu, J.; Yu, R.; Lou, J.; Yang, M.; Yao, Z.; et al. New Crosslinked Hyaluronan Gel for the Prevention of Intrauterine Adhesions after Dilation and Curettage in Patients with Delayed Miscarriage: A Prospective, Multicenter, Randomized, Controlled Trial. J. Minim. Invasive Gynecol. 2019, 26, 94–99. [Google Scholar] [CrossRef]
  40. Zhou, Q.; Shi, X.; Saravelos, S.; Huang, X.; Zhao, Y.; Huang, R.; Xia, E.; Li, T.C. Auto-cross-linked hyaluronic acid gel for prevention of intrauterine adhesions after hysteroscopic adhesiolysis: A randomized controlled trial. J. Minim. Invasive Gynecol. 2021, 28, 307–313. [Google Scholar] [CrossRef]
  41. U.S. Environmental Protection Agency. Provisional Peer-Reviewed Toxicity Values for Hydrazine. 2009. Available online: https://hhpprtv.ornl.gov/issue_papers/Hydrazine.pdf (accessed on 12 May 2020).
Jcm 11 00931 g001 550
Figure 1. Chemical structure of hyaluronic acid-based polymers.
Figure 1. Chemical structure of hyaluronic acid-based polymers.
Jcm 11 00931 g001
Jcm 11 00931 g002 550
Figure 2. Synthesis of hyaluronic acid auto-crosslinked polymer gel (Hyalobarrier®).
Figure 2. Synthesis of hyaluronic acid auto-crosslinked polymer gel (Hyalobarrier®).
Jcm 11 00931 g002
Jcm 11 00931 g003 550
Figure 3. Synthetic route of hyaluronic acid crosslinked polymers B and C (HyaRegen® and MateRegen®).
Figure 3. Synthetic route of hyaluronic acid crosslinked polymers B and C (HyaRegen® and MateRegen®).
Jcm 11 00931 g003
Jcm 11 00931 g004a 550Jcm 11 00931 g004b 550
Figure 4. Comparison of physical characteristics of hyaluronic acid gels. (a) Comparison of viscosity vs. shear rate flow curves for gel A (Hyalobarrier®) and gels B and C (HyaRegen® and MateRegen®). (b) Comparison of storage moduli G’ versus frequency for hyaluronic acid-based products.
Figure 4. Comparison of physical characteristics of hyaluronic acid gels. (a) Comparison of viscosity vs. shear rate flow curves for gel A (Hyalobarrier®) and gels B and C (HyaRegen® and MateRegen®). (b) Comparison of storage moduli G’ versus frequency for hyaluronic acid-based products.
Jcm 11 00931 g004aJcm 11 00931 g004b
Jcm 11 00931 g005 550
Figure 5. Peel strength comparison between hyaluronic acid gels.
Figure 5. Peel strength comparison between hyaluronic acid gels.
Jcm 11 00931 g005
Jcm 11 00931 g006 550
Figure 6. Photographs of peel strips after completing two peel strength tests on all three polymers.
Figure 6. Photographs of peel strips after completing two peel strength tests on all three polymers.
Jcm 11 00931 g006
Jcm 11 00931 g007 550
Figure 7. Comparison of average extrusion forces between HA gels in their commercial syringes.
Figure 7. Comparison of average extrusion forces between HA gels in their commercial syringes.
Jcm 11 00931 g007
Table
Table 1. Description of the products.
Table 1. Description of the products.
Auto-Crosslinked Polymer ACrosslinked Polymers
BC
Hyalobarrier®HyaRegen®MateRegen®
Syringe filling (mL)1010/205
Claimed HA concentration (mg/mL)305N/A
Shelf life3 years2 years2 years
Storage conditions2–8 °C2–30 °C2–30 °C
N/A: not available.
Table
Table 2. Summary of the evaluated physical characteristics of the products.
Table 2. Summary of the evaluated physical characteristics of the products.
Polymers
ABC
Shear viscosity (Pa.s−1)1143836
Storage modulus G’ (Pa)1001620
Peel strength0.016 lbf
72 mN		0.0089 lbf
39.6 mN		0.0086 lbf
38.3 mN
Extrusion force 4.5 lbf
20 N		6.33 lbf
28 N		3.79 lbf
17 N
lbf: pound-force; mN: milli-Newton; N: Newton; Pa: Pascal; Pa.s−1: Pascal-seconds.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Torres-de la Roche, L.A.; Bérard, V.; de Wilde, M.S.; Devassy, R.; Wallwiener, M.; De Wilde, R.L. Chemically Modified Hyaluronic Acid for Prevention of Post-Surgical Adhesions: New Aspects of Gel Barriers Physical Profiles. J. Clin. Med. 2022, 11, 931. https://doi.org/10.3390/jcm11040931

AMA Style

Torres-de la Roche LA, Bérard V, de Wilde MS, Devassy R, Wallwiener M, De Wilde RL. Chemically Modified Hyaluronic Acid for Prevention of Post-Surgical Adhesions: New Aspects of Gel Barriers Physical Profiles. Journal of Clinical Medicine. 2022; 11(4):931. https://doi.org/10.3390/jcm11040931

Chicago/Turabian Style

Torres-de la Roche, Luz Angela, Véronique Bérard, Maya Sophie de Wilde, Rajesh Devassy, Markus Wallwiener, and Rudy Leon De Wilde. 2022. "Chemically Modified Hyaluronic Acid for Prevention of Post-Surgical Adhesions: New Aspects of Gel Barriers Physical Profiles" Journal of Clinical Medicine 11, no. 4: 931. https://doi.org/10.3390/jcm11040931

APA Style

Torres-de la Roche, L. A., Bérard, V., de Wilde, M. S., Devassy, R., Wallwiener, M., & De Wilde, R. L. (2022). Chemically Modified Hyaluronic Acid for Prevention of Post-Surgical Adhesions: New Aspects of Gel Barriers Physical Profiles. Journal of Clinical Medicine, 11(4), 931. https://doi.org/10.3390/jcm11040931

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop