Cholesterol Dissolution Rate in Micellar Bile Acid Solutions: Retarding Effect of Added Lecithin

Higuchi, William I.; Prakongpan, Sompol; Surpuriya, Vijay; Young, Fudah

doi:10.1126/science.178.4061.633

Cited by 51 publications

(17 citation statements)

References 10 publications

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“…When slow cholesterol transfer occurs at the cholesterol monohydrate crystal-solution interface, P may be considered to be a first-order reaction rate constant associated with this rate-determining process (1). If the process involves the slow solubilization of the aqueous free cholesterol by the micelles in the diffusion layer, P has an entirely different meaning.…”

Section: Equationmentioning

confidence: 99%

Dissolution Rate Studies of Cholesterol Monohydrate in Bile Acid–Lecithin Solutions Using the Rotating‐Disk Method

Prakongpan

Higuchi

Kwan

et al. 1976

Journal of Pharmaceutical Sciences

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Section: Equationmentioning

confidence: 99%

Dissolution Rate Studies of Cholesterol Monohydrate in Bile Acid–Lecithin Solutions Using the Rotating‐Disk Method

Prakongpan

Higuchi

Kwan

et al. 1976

Journal of Pharmaceutical Sciences

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“…4. The decrease of dissolution rate on the 'addition of lecithin, which has also been observed bv others (13)(14)(15), is counter to that expected from the increased solubility of cholesterol caused by the addition of lecithin. No single step controls dissolution in this region.…”

Section: And Discussionmentioning

confidence: 48%

“…Thus the results are most conveniently described in terms of three regions: stagnant bile, slow bile flow, and fast bile flow. Previous studies have been hampered because these regions have not been adequately defined (13)(14)(15). As a result, the different mechanisms involved have not been delineated.…”

Section: And Discussionmentioning

confidence: 99%

Accelerating Gallstone Dissolution

Tao

Cussler

Evans

1974

Proc. Natl. Acad. Sci. U.S.A.

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The dissolution rates of cholesterol in model bile salt solutions are controlled by diffusion in slowly flowing bile and by interfacial kinetics in rapidly flowing bile. At low flow, dissolution varies with the square root of bile flow and can be predicted, apriori, from existing correlations of mass transfer. At high bile flow, dissolution is independent of bile flow and is probably dominated by the rate of micelle adsorption. These results show that cholesterol gallstone dissolution, a potential nonsurgical therapy for cholelithiasis, can be accelerated little in slow bile, but more significantly in rapidly flowing bile.

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“…CONCLUSIONS AND PHYSIOLOGICAL IMPLICATIONS Investigation of the dissolution of both cholesterol monohydrate and human gallstones by both bile salts and bile salt lecithin mixed media by Higuchi and coworkers (17,18) has shown that the dissolution is interfacially controlled. It was observed in these studies that the addition of lecithin to the dissolution media containing the bile salt reduced the dissolution rates even though it increased the equilibrium solubility of cholesterol monohydrate in the dissolution media (19). Hoelgaard and Frokajaer (20) have shown that the decrease in dissolution rates observed in the presence of added lecithin is primarily due to the adsorption of lecithin on the surface of cholesterol crystals.…”

Section: Resultsmentioning

confidence: 98%

Kinetics and Thermodynamics of Dissolution of Lecithin by Bile Salts

Lindenbaum

Rajagopalan

1984

Hepatology

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The kinetics of dissolution of dispersions of egg phosphatidylcholine (lecithin) by bile salts WBS studied by observing the decrease in turbidity as mixed micelles of lecithin and bile salts were formed. The rate of dissolution of lecithin corresponding to formation of mixed micelles was studied in the presence of dihydroxy bile salts, sodium deoxycholate, sodium chenodeoxycholate, sodium ursodeoxycholate and one trihydroxy bile salt, sodium cholate. The rate of dissolution of lecithin and mixed micelle formation decreased in the order: chenodeoxycholate > deoxycholate cholate > ursodeoxycholate. Kinetic solvent isotope studies in DzO, along with measurement of enthalpies of mixed micelle formation both in HzO and DzO, suggest that formation and stabilization of mixed micelles are related to "hydrophobicity" as estimated by high performance liquid chromatography retention factors.On the basis of phase equilibrium and X-ray diffraction studies, a generally accepted model for the bile saltlecithin mixed micelle was proposed by Small (1, 2) and Dervichian (3). According to this model, a disc-shaped micelle is formed on the association of lecithin with bile salt. The disc core consists of hydrocarbon alkyl chains of the lecithin molecules surrounded by a ring of bile salt molecules. Thus, the disc-shaped micelle exterior presents to the aqueous solvent only the hydrophilic end groups of the lecithin and the hydrophilic sides of the bile salt.Whereas it is generally agreed that mixed micelles occur in these solutions, there remains controversy concerning their detailed structure. Mazer and coworkers (4) have suggested that their quasielastic light scattering data (QLS) can best be interpreted in terms of a mixed disc model. This model preserves the disc-shaped mixed micelle of Small and Dervichian but also requires the presence of some bile salt molecules within the interior of the micelle. These bile salt molecules within the micelle interior are presumed to exist as hydrogen-bonded dimers. Calorimetrically derived exothermic heats of mixed micelle formation have also been interpreted to support this model (5). Recently, Muller (6) has proposed another modification to the mixed micelle model. On the basis of X-ray small angle scattering data, Muller suggests that structural dimorphism exists in bile salt leci- The purpose of this study was to attempt to shed further light on the process of mixed micelle formation by measuring the rate of dissolution of lecithin in bile salt solutions.The kinetics of mixed micelle formation were followed by studying the time-dependent decrease in turbidities of a dispersion of lecithin (L) after addition of a given bile salt (BS) solution (9). In the course of the reaction multilamellar L interacts with BS to form mixed micelles M L + B S e M

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Cholesterol Dissolution Rate in Micellar Bile Acid Solutions: Retarding Effect of Added Lecithin

Cited by 51 publications

References 10 publications

Dissolution Rate Studies of Cholesterol Monohydrate in Bile Acid–Lecithin Solutions Using the Rotating‐Disk Method

Dissolution Rate Studies of Cholesterol Monohydrate in Bile Acid–Lecithin Solutions Using the Rotating‐Disk Method

Accelerating Gallstone Dissolution

Kinetics and Thermodynamics of Dissolution of Lecithin by Bile Salts

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