Abstract

Pectin binds the mesothelial glycocalyx of visceral organs, suggesting its potential role as a mesothelial sealant. To assess the mechanical properties of pectin films, we compared pectin films with a less than 50% degree of methyl esterification (low-methoxyl pectin, LMP) to films with greater than 50% methyl esterification (high-methoxyl pectin, HMP). LMP and HMP polymers were prepared by step-wise dissolution and high-shear mixing. Both LMP and HMP films demonstrated a comparable clear appearance. Fracture mechanics demonstrated that the LMP films had a lower burst strength than HMP films at a variety of calcium concentrations and hydration states. The water content also influenced the extensibility of the LMP films with increased extensibility (probe distance) with an increasing water content. Similar to the burst strength, the extensibility of the LMP films was less than that of HMP films. Flexural properties, demonstrated with the 3-point bend test, showed that the force required to displace the LMP films increased with an increased calcium concentration (p < 0.01). Toughness, here reflecting deformability (ductility), was variable, but increased with an increased calcium concentration. Similarly, titrations of calcium concentrations demonstrated LMP films with a decreased cohesive strength and increased stiffness. We conclude that LMP films, particularly with the addition of calcium up to 10 mM concentrations, demonstrate lower strength and toughness than comparable HMP films. These physical properties suggest that HMP has superior physical properties to LMP for selected biomedical applications.

Highlights

  • A variety of polysaccharide polymers have been implicated in biomedical applications, including alginate [1], cellulose [2], chitin [3], agarose [4], and pectin [5]

  • Unique to Low-methoxyl pectins (LMP) films, the addition of calcium during preparation resulted in LMP films that were significantly thicker than high-methoxyl pectins (HMP) films (p < 0.05) (Figure 1E)

  • We studied the physical properties of LMP relevant to its role as a mesothelial sealant

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Summary

Introduction

A variety of polysaccharide polymers have been implicated in biomedical applications, including alginate [1], cellulose [2], chitin [3], agarose [4], and pectin [5]. Pectin is a interesting polysaccharide because of its structural and functional features. Commercial pectins contain primarily linear chains of homogalacturonan, a partially methyl esterified polymer of Molecules 2020, 25, 75; doi:10.3390/molecules25010075 www.mdpi.com/journal/molecules (1-4)-α-D-galacturonic acid (GalA) [6], along with lesser amounts of rhamnogalacturonan [7]. Pectin in plants is more complex, with regions of homogalacturonan covalently linked to the branched pectic polymers rhamnogalacturonan I and rhamnogalacturonan II [8] and to arabinogalactan proteins [9]. Pectin demonstrates remarkable adhesivity to gut mucins, providing a useful mechanism for oral drug delivery [10]. Pectin binds the mesothelial glycocalyx of visceral organs [5], suggesting its potential role as a mesothelial sealant [11]

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