2010
DOI: 10.1016/j.msec.2010.05.002
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Degradation of sulfated polysaccharide extracted from algal Laminaria japonica and its modulation on calcium oxalate crystallization

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Cited by 19 publications
(13 citation statements)
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“…Currently, the main prescription drugs for treatment of urinary calculi are citrate, magnesium preparations, orthophosphate, allopurinol, and thiazide diuretics. However, the action mechanism of these drugs remains unclear, and their curative effects can be marginal [ 13 ]. Thus, scholars must develop new highly efficient, nontoxic, and inexpensive anti-stone drugs for scientific and practical applications [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…Currently, the main prescription drugs for treatment of urinary calculi are citrate, magnesium preparations, orthophosphate, allopurinol, and thiazide diuretics. However, the action mechanism of these drugs remains unclear, and their curative effects can be marginal [ 13 ]. Thus, scholars must develop new highly efficient, nontoxic, and inexpensive anti-stone drugs for scientific and practical applications [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…Not every anionic molecule can interact with the oxalate crystals and interfering with their formation [29]. However, when they interact with the crystals, changes in the morphology [14,15] and size of the crystals can occur [16,17,29]. For example, Wesson and collaborators [29] demonstrated that anionic proteins tend to increase the number of crystals and decrease their size since these negatively charged proteins interact more with the rich calcium faces of both COM and COD crystals, blocking their growth.…”
Section: Resultsmentioning
confidence: 99%
“…The studies are done in vitro as well as with cells under culture conditions and in vivo. The data are well reviewed in a recently published paper [13], which verifies these polymers can inhibit the formation of CaOx renal stone formation in different ways: they inhibit crystallization (both in the nucleation phase [14,15,16] and in growth phase [16,17]); they inhibit the aggregation phase [14,15,16,17,18]; they inhibit the occurrence of COM crystals and the transformation of COM to COD [14,16,17,18]; and they inhibit renal tubular cell injury in vivo [19,20,21].…”
Section: Introductionmentioning
confidence: 99%
“…C 6 S is the major component of GAGs responsible for their inhibitory effect. The inhibitory mechanisms of C 6 S include the following [38].

C 6 S is a linear polysaccharide polyanion.

…”
Section: Resultsmentioning
confidence: 99%