Crystal sedimentation and stone formation
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- Baumann, J.M., Affolter, B. & Meyer, R. Urol Res (2010) 38: 21. doi:10.1007/s00240-009-0239-8
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Mechanisms of crystal collision being the first step of aggregation (AGN) were analyzed for calcium oxalate monohydrate (COM) directly produced in urine. COM was produced by oxalate titration in urine of seven healthy men, in solutions of urinary macromolecules and in buffered distilled water (control). Crystal formation and sedimentation were followed by a spectrophotometer and analyzed by scanning electron microscopy. Viscosity of urine was measured at 37°C. From results, sedimentation rate (vS), particle diffusion (D) and incidences of collision of particles in suspension by sedimentation (IS) and by diffusion (ID) were calculated. Calculations were related to average volume and urinary transit time of renal collecting ducts (CD) and of renal pelvis. vS was in urine 0.026 ± 0.012, in UMS 0.022 ± 0.01 and in control 0.091 ± 0.02 cm min−1 (mean ± SD). For urine, a D of 9.53 ± 0.97 μm within 1 min can be calculated. At maximal crystal concentration, IS was only 0.12 and ID was 0.48 min−1 cm−3 which, even at an unrealistic permanent and maximal crystalluria, would only correspond to less than one crystal collision/week/CD, whereas to the same tubular wall being in horizontal position 1.3 crystals/min and to a renal stone 624 crystals/cm2 min could drop by sedimentation. Sedimentation to renal tubular or pelvic wall, where crystals can accumulate and meet with a tissue calcification or a stone, is probably essential for stone formation. Since vS mainly depends on particle size, reducing urinary supersaturation and crystal growth by dietary oxalate restriction seems to be an important measure to prevent aggregation.
KeywordsCalcium oxalate Sedimentation Diffusion Collision Aggregation
Nephrolithiasis can start from sub-micron particles of organic material complexed with amorphous hydroxyapatite, which after erosion to the papillary surface provide a platform to which crystals formed in the urine can attach . Much work was done to elucidate this initial phase of nephrolithiasis [2, 3]. However, for the transformation of kidney calcifications to a clinically symptomatic stone, further crystal apposition is necessary. It probably occurs during crystalluria by crystal aggregation (AGN) [4, 5]. Crystallization processes involved in stone formation are, apart from urinary supersaturation, essentially influenced by crystallization inhibitors like citrate and urinary macromolecules (UM), the latter comprising a large group of proteins and some glycosaminoglycans . Physical chemistry has much contributed to a better understanding of stone disease . Whereas nucleation and growth of crystals follow relative simple physico-chemical rules, AGN is more difficult to describe. In order to aggregate, particles have to collide with each other and then to be united by Van der Waals forces, viscous binding or, as recently shown, by the formation of solid calcium (Ca) bridges . In suspensions not being stirred or shaken, particle collision can still occur by thermal diffusion or during sedimentation of particles with different sedimentation rates. Sedimentation or diffusion to walls of renal tubules or pelvis where crystals are retained by fluid drag  or attached to the tissue  is another mechanism enhancing particle collision. An equation describing AGN exclusively based on diffusion and with an unlimited size of aggregates has been developed by Smoluchowski . However, in urine where AGN is inhibited by UM, aggregates are limited to a few crystals . Sedimentation at rates increasing with particle size was frequently determined as indicator for AGN [12, 13] but its role in a first step of crystal AGN has been neglected. The aim of this study was to evaluate the importance of the different mechanisms of crystal collision and to show how they could be influenced by stone metaphylaxis. Sedimentation rate (vS) of calcium oxalate was measured in urine and the corresponding UM solutions (UMS) where crystals were produced directly and AGN was found to be extremely rare owing to a high inhibitory activity. Thermal diffusion, which cannot easily be observed, was calculated after measurement of fluid viscosity and crystal dimensions, both being responsible for particle friction during sedimentation and diffusion. From these parameters and vS the incidence of crystal collisions was calculated in suspension as well as on walls of renal collecting ducts, where stone formation may start by the retention of big aggregates  and in the renal pelvis, where stones grow to an obstructing size.
Materials and methods
Spot urine of seven healthy men of the staff with no previous history of stones was collected in the morning after high fluid intake on free diet, divided into three portions and, without further treatment, immediately was used for the isolation of UM, crystallization tests and viscosimetry.
Preparation of UMS
55 cm3 of urine were injected into the dialysis fluid compartment of a capillary hemodialyser (Hemoflow F3, Fresenius AG, Bad Homburg, Germany), the exclusion limit of the dialysis membrane being 5 kDa. The compartment was closed and the urine dialysed against 12 L (200 cm3/min) of deionized water .
Crystallization tests and scanning microscopy
Mean vS was calculated from individual vS and not from mean dOD/dt and mean mOD because these parameters are interdependent.
After sedimentation, particles were resuspended and millipore filtered (pore size 0.45 μm). Crystals and aggregates retained on the filters were visualised by a LEO 430 scanning electron microscope.
Kinematic viscosities of urine, UMS and buffered distilled water (control) were determined in triplicate by an Ubbelohde Micro Viscosimeter (Schott-Geräte GmbH, Mainz, Germany) at 37°C. To get the dynamic viscosity (η) used for the different calculations, results of viscosimetry were multiplied by the density of solutions at 37°C (ρSOL = 0.994 g cm−3) and expressed in g cm−1 min−1.
To facilitate calculations all constants were also indicated within brackets in units of g, cm and min.
Sedimentation rate (vS)
Incidence of collision in suspension by diffusion (ID)
Incidence of collision in suspension by sedimentation (IS)
Calculations of IS were performed for varying ratio rL/r, an average C of 10,000 cm−3 and a log (CL/C) given by the empirical expression −1.7 (rL/r − 1). These parameters were derived from measurements of volume/particle-size ratios in urine of stone patients and controls .
Incidence of collision with fixed particle (IF)
Sedimentation on unit surface (S)
Crystal accumulation by sedimentation in a horizontally positioned tubule (A)
All calculations were performed for the mean r obtained by sedimentation experiments in urine (1.13 μm) and, with the exception of calculations by Eq. 6, for a maximal crystal concentration during crystalluria of 24,000 cm−3 . For renal collecting ducts an average L of 2.7 cm, R of 25 × 10−4 cm and tT of 0.82 min were used . For the renal pelvis an average volume of 7 cm3 and a tT of 12 min were assumed . Statistical analyses were performed by Student’s t test.
Crystallization experiments, determination and calculation of vS
Calculation of crystal motion in suspension
Motion of crystals by sedimentation and by diffusion in urine and UMS during average transit time in the kidney (3 min) and the renal pelvis (12 min) (calculated for crystals with r = 1.13 μm and q = 1.14, mean ± SD, n = 14)
Kidney after 3 min
Renal pelvis after 12 min
0.79 ± 0.35
0.017 ± 0.002
3.15 ± 1.40
0.033 ± 0.003
0.65 ± 0.21
0.017 ± 0.001
2.59 ± 0.83
0.035 ± 0.002
Calculation of crystal collision and accumulation
Incidence of crystal collision by diffusion at concentration 24,000/cm3 and by sedimentation at 10,000/cm3 in average collecting duct (CD, Volume = 5.3 × 10−5 cm3) and renal pelvis (Volume = 7 cm3) and crystal accumulation by sedimentation at concentration 24,000/cm3 in CD being in horizontal position or on renal stone surface, as calculated for crystals with r = 1.13 μm and q = 1.14
2.5 × 10−5
6.7 × 10−6
Crystals/min in horizontal CD
Crystals/min on cm2 stone surface
However, sedimentation was found to be efficient especially for crystal accumulation (Table 2). For a C of 24,000 cm−3 and a vS of 0.026 cm min−1S amounted to 624 min−1 cm−2. Within an average transit time of 12 min through a renal pelvis, this S would correspond to the deposition of 7,500 crystals on 1 cm2 of a stone surface. For an identical crystalluria in a CD an accumulation rate A of 1.35 min−1 was calculated, which means that at least one crystal per minute could be accumulated by sedimentation in a horizontally positioned collecting duct.
For non-spherical particles like crystals, current physico-chemical equations for sedimentation and diffusion have to be adapted by a dimension related correcting factor (q) and by a volume related virtual radius (r). Values for q and r are available for ellipsoid particles  but not for crystals. The parameters q and r determine together with η particle friction in solutions (f = 6πqrη), which also is not known for crystals. Therefore, the aim of our crystallization experiments was to demonstrate that modification of equations for sedimentation and diffusion derived for ellipsoids principally also can be applied for crystals. By slow oxalate titration we produced rhomboid crystals showing maximal deviation from spherical particles. Results of experimentally obtained vS were then compared with those calculated from crystal volume and shape being aware that both methods imply some difficulties. Determining volumes from 2-dimensional pictures is problematic. Also sedimentation measurement poses several problems. Determining vS is based on the extrapolation of the drop of OD being only in its initial part linear . To avoid major turbidity due to flocculation of Tamm Horsfall glycoprotein (THG) or due to solid material other than the calcium oxalate crystals produced, we used freshly voided warm urine under a diuresis of at least 100 cm3/h. Especially high ionic strength is known to provoke the polymerization of THG . Slow oxalate titration was performed because it produces in UMS and urine crystal populations of a rather homogenous size and shape as observed in the control . The minimal difference observed between calculated and experimentally determined vS showed that r and q seem to be adequate to describe sedimentation and diffusion of crystals.
To be relevant for nephrolithiasis, results of crystallization tests and calculations have to be discussed in view of crystal concentrations actually found in urine, of renal anatomy and of urinary transit times through kidneys and the upper urinary tract. Total crystal concentrations are thought to vary during crystalluria between 7,200 and 24,000 crystals per cm3 . Crystal size shows big variations and increases during renal passage by crystal growth in supersaturated urine [16, 19]. The capacity of renal tubules is in the order of a few cubic micrometers  and that of a renal pelvis in the order of several cubic centimeters . But tubular dimensions vary between the different nephrons [9, 16]. Urinary transit times in the kidney are 2–4 min  and in the renal pelvis on average 12 min depending on diuresis . Near tubular walls the passage of small crystals may be delayed up to more than 1 h by special hydro-dynamic factors like fluid drag or sticking to the wall . Being aware of all these anatomical and physiological complexities, for the calculations we used maximal crystal concentrations and average renal tubular and pelvic parameters found in current literature. Crystal friction and adhesion to tubular wall being difficult to quantify were neglected. Despite of all limitations and simplifications the following conclusions may be drawn from our study. The extremely low values of ID and IS demonstrate that AGN of free particles can hardly occur in the renal tubular system. Big aggregates observed in urine of some stone patients  may rather originate from the renal pelvis or the bladder, when crystals collide on a pelvic or bladder wall after sedimentation during a prolonged urinary residence time. As our calculations of crystal accumulation by sedimentation show, a similar but less extensive mechanism can be operative in renal tubules. Crystals, already formed in proximal tubules after high oxalate ingestion [9, 16], may undergo sedimentation to tubular walls being in horizontal position, where they may meet other crystals whose passage is delayed by fluid drag or adhesion to renal tissue. The latter mechanism may explain large aggregates found in CD near papillary surface . During crystalluria, crystal collisions after sedimentation on tubular or pelvic walls seem to be more likely than in free solution.
It may look tentative to draw conclusions from our calculations on stone frequencies being on average only 1 stone/7 years. However, severe crystalluria occurs only occasionally and crystal deposits may be pushed out with urine flow or overgrowth by the tubular epithelial cells with subsequent removal by macrophages . Furthermore, as shown again in this study, UM like THG are potent inhibitors and essentially influence AGN of Ca oxalate . Their effect was especially pronounced in our study since the experimental conditions allowed the use of urine without previous removal of THG by centrifugation or filtration . Therefore, on our SEM pictures aggregates hardly could be found in urine and UMS despite of intensive crystal collisions promoted by stirring during oxalate titration. UM are known to coat crystals  and thus to reduce crystal surfaces disposable for the apposition of other crystals . This high inhibitory effect of UM may explain the fact that incidence of nephrolithiasis is much lower than could be expected from the widespread occurrence of crystalluria and kidney calcifications . It also may explain the slow growth that is often observed for stone residues after ESWL as well as for kidney stones. Several groups have shown that urine of some stone formers is less capable of inhibiting crystal aggregation and that its ability to inhibit crystal aggregation decreases in direct proportion to the frequency of stone recurrence [12, 24].
Our equations show that crystal concentration (C) and sedimentation rate (vS), the latter being a function of crystal size or the virtual crystal radius (r), respectively, are the most important factors which influence crystal collision by sedimentation. Provided that sedimentation and AGN are important for stone disease, dietary oxalate restriction and an increased fluid intake, both reducing urinary supersaturation and crystal growth, seem to be essential for stone metaphylaxis. Also the consumption of an acid load (a load of animal protein without high alkali consumption) is a risk for relative hyperoxaluria . After a dietary oxalate load, the incidence of large urinary crystals and in stone patients also of aggregates markedly increased [9, 19]. On the other hand, in renal collecting ducts and pelvis, C and urinary transit time during which sedimentation can occur are reduced by an increased diuresis [16, 17]. Recent studies showed that the benefit of an increased urine volume largely seems to outweigh the concomitant loss of inhibition of AGN observed after UM dilution [14, 26].
Our experiments show that adaptations of equations for sedimentation and diffusion derived for ellipsoid particles also can be used for crystals. Calculations by these equations demonstrate, that crystal sedimentation, contrary to diffusion, seems to be most important for crystal collision being a first step of crystal AGN and thus for stone formation during crystalluria. Most collisions may occur in renal tubules where, if they are in horizontal position, crystals accumulate by sedimentation and in renal pelvis by crystal sedimentation on pre-existing stones. The chance for the formation of free aggregates in the renal tubular system seems to be rather poor. Since sedimentation rate increases with crystal size in square, all measures reducing crystal formation and growth are most important to prevent AGN.
This work was supported by Vinetum Foundation, Biel, Switzerland. Scanning microscopy was performed at the Division for SEM, Berne University of Applied Sciences, Burgdorf, Switzerland.
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