Method for making uniformly sized particles from water-insoluble organic compounds.

BACKGROUND OF THE INVENTION

0001Particles of compounds having low water-solubility are commonly used in a wide variety of applications, including ceramics, paints, inks, dyes, lubricants, pesticides, insecticides, fungicides, fertilizers, chromatography columns, cosmetics, lotions, ointments, and detergents. Aqueous dispersions of particles are used in many cases to avoid hazards such as flammability and toxicity associated with organic solvents. Such dispersions typically have a broad range of particle size.

0002In many cases product performance is improved by controlling the particle size distribution. In general, smaller particles of a compound will dissolve faster than larger particles of the same compounds. Control of particle size is, therefore, important in controlling the rate of solubilization.

0003Many drugs have been formulated as particles for controlled-release following oral administration or, implantation. Particle size is one important factor affecting .the release rate of these drugs. Those skilled in the art can discern other examples for using particle size to control product performance for the substances listed above.

0004Drugs that are insoluble in water can have significant benefits when formulated as a stable suspension of particles of less than three microns diameter. In this particulate form, the drug can be injected intravenously, circulate in blood, and be preferentially accumulated in, for example, the reticuloendothelial system, where it can facilitate normal reticuloendothelial functions such as detoxification. Alternatively, the drug can reside in the reticuloendothelial cells where it is stored until solubilized or metabolized into an active form which circulates in blood' to other tissues for efficacy. This "slow" release of active drug can provide more constant drug concentrations in plasma over a period of hours, days, weeks, or months, resulting in improved therapeutic efficacy. Biodegradable particles which are radiopaque or labelled with a radioisotope are useful for diagnostic imaging of organs, such as liver and spleen, with high concentrations of fixed reticuloendothelial function.

0005Many advantages have already been recognized for insoluble particulate radiopaque contrast media, for example, as explained in "Improvement in Radiographic Contrast Media Through the Development of Colloidal or Particulate Media: an Analysis", by Harry W. Fischer, Journal of Theoretical Biology, 67: 653-670 (1977). More recent papers on this subject include Violante, M. R., Fischer, H. W., and Mahoney, J.A., "Particulate Contrast Media," Invest. Radiol., 15: S329 November-December 1980; and Violante, M. R., Dean, P. B., Fischer, H. W., and Mahoney, J. A., "Particulate Contrast Media for Computer Tomographic Scanning of the Liver", Invest. Radiol., 15: 171 November-December 1980.

0006There are enormous medical implications for the intravenous administration of drugs formulated as suspensions of particles of three microns diameter, or less, which can be accumulated by phagocytic cells and slowly solubilized for sustained release into plasma for circulation to other organs ; and tissues. Obvious drug classes appropriate for formulation as particulate suspensions include: antineoplastics, antimicrobials, antivirals, anticoagulants, antihypertensives, antihistamines, antimalarials, male and female contraceptives, antiepileptics, depressants and antidepressants, adrenocortical steroids, hormones and hormone antagonists, cardiac glycosides, immunosuppressants, beta-blockers, water-insoluble vitamins, sympathomimetics, hypoglycemic agents, hyperglycemic agents, analgesics, tranquilizers, mood altering drugs, and others. The treatment of deficiency diseases, alcohol abuse, drug abuse, and many others could be improved with intravenous administration of particulate suspensions of the appropriate drug. Other medical applications for particulate drug suspensions will be apparent to those skilled in the art.

0007Accurate control of particle size is essential for safe and efficacious use of these formulations. Particles must be less than three microns in diameter to safely pass through capillaries without causing emboli..This is critical for intravenous administration since the particles must pass through lung capillaries before reaching the fixed reticuloendothelial cells of liver and spleen. Restriction to particle diameters of 0.01-0.1 micron could result in selective accumulation of these particles in certain tissues, eg., neoplastic tissue, where capillaries are somewhat more porous than capillaries of normal tissues. Suspensions of particles with diameters greater than 10 microns could be useful for selective intra-arterial administration to purposely embolize vessels feeding abnormal tissue such as a neoplasm. Accurate and precise control of particle diameters is essential for efficacy while minimizing or avoiding adverse effects in each of these applications.

0008Conventional methods of making water-insoluble compounds produce particles of many different sizes, many of which are unsuitable for the purpose at hand. Mechanically sorting or separating a desired particle size from a mix of sizes is difficult and unsatisfactory. Centrifuging and filtration do not produce high yields of particles that are all precisely the same desired size.

0009Investigations of water-insoluble radiopaque contrast materials required uniform particles in specific sizes that were very difficult to obtain by conventional methods. Precipitation as a way of directly forming particles of a predetermined size was then investigated. Partial success was achieved with one material and one method as reported in "Particulate Contrast Media", Investigative Radiology, 15: S329 November-December 1980; but this method would not work with other materials and would not allow accurate variation and control of the particle size produced.

0010Further investigation led to the invention of this application, which is effective with any drug or other compound having a solubility in water of-preferably less than .one part per ten thousand to obtain a predetermined particle .size of the water-insoluble drugs or other compounds used in aqueous dispersions.

SUMMARY OF THE INVENTION

0011The invention involves a method of making uniformly sized particles of a solid, water-insoluble organic compound by, first, preparing a solution of the solid organic compound in a water-miscible organic solvent for the compound, the compound having essentially little aqueous solubility; second, infusing an aqueous precipitating liquid into the solution at a temperature between about -10°C and about 100°C and at an infusion rate of from about 0.01 ml per minute to about 1000 ml per minute per unit volume of 50 ml to produce a suspension of precipitated solid organic compound in the form of substantially non-aggregated particles with a substantially uniform mean particle diameter selected from the range of less than about 10 microns, such that the particle size is directly related to the solution temperature and inversely related to infusion rate, and then separating the particles from the organic liquids and washing in aqueous washing liquid. Agitation of the solution being infused with precipitating liquid is preferred. This can be accomplished by stirring, shaking, combining two streams of liquid, by the infusing itself and by other techniques known to those skilled in the art.

0012In preferred embodiments of the invention, additional aqueous precipitating liquid is added to the suspension before the particles are separated from the organic solvents. Separation can be accomplished, for example, by centrifugation, membrane filtration, reverse osmosis, or other methods.

0013The aqueous washing liquid can be the same as the aqueous precipitating liquid, and it can be pharmaceutically acceptable for injecting into a patient.

0014The aqueous precipitating liquid can be water, a solution of a mineral salt, or a surfactant solution. Suitable aqueous surfactant solutions include 5% polyvinyl pyrrolidone C-30, 0.1% polyvinyl pyrrolidone C-15, 0.1% human serum albumin, 0.1% Pluronic F-68 (poloxamer 188), and 0.33% gelatin, alone or combined with 0.6% hetastarch, 0.02% propylene glycol, or 2% sucrose. The aqueous precipitating liquid can be infused through a needle of standard gauge.

0015The mean particle diameter of the particles can be up to about 10 microns, preferably in a range of 0.01 microns to about 5 microns.

0016Particles made according to this invention will typically have a particle size distribution with a maximum relative standard deviation of 50%, for example 95% of the particle having a mean size of 1.0 micron will be within the size range of 0.5 to 1.5 microns.

0017The solid organic compound has, preferably, an aqueous solubility of less than about one part per ten thousand, and the compound may be organo-metallic. Generally, any compound that meets the other requirements of the invention is suitable, including many drugs. Where heparin complexes are used, no surfactant is necessary.

0018The organic solvent can be dimethyl sulfoxide, dimethyl formamide, N,N'-dimethyl acetamide, phenol, isopropanol, or other solvents.

0019In a preferred embodiment, the method includes the additional step of diluting the-organic solution with a non-solvent liquid such that the ratio of non-solvent to solvent is between about 100:1 and about 1:100, after preparing the organic solution and before the infusion step, so that the particle size is directly related to the ratio of non-solvent to solvent.

0020In further preferred embodiments, the non-solvent, in one in which the organic compound is slightly more soluble than in water. The non-solvent can be a lower aliphatic alcohol.

0021In particular preferred embodiments, iodipamide ethyl ester, an ethyl ester of a triiodobenzoic acid derivative, is dissolved in dimethyl sulfoxide and diluted with ethanol; if the ratio of ethanol to dimethyl sulfoxide is greater than about two, the mean particle diameter is greater than about one micron, and if the ratio of ethanol to dimethyl sulfoxide is less than about two, the mean particle diameter is less than about one micron.

BRIEF DESCRIPTION OF THE DRAWINGS

0022<ul id="ul0001" list-style="none"><li>Figure 1 is a graph of free energy of the various phases of the compounds used in the invention.</li><li>Figure 2 is a graph of the relationship between size distribution of particles and time interval between onset and completion of precipitation.</li><li>Figure 3 is a graph of infusion rate (ml/min.) (of aqueous precipitating liquid) as a function of the product of stir rate (rpm) and total volume (liters) of the organic solution at a constant temperature; the relationship: aqueous infusion rate (ml/min.) = 23 + 0.14 [stir rate (rpm) x volume organic solution (1) defines the parameters for production of iodipamide ethyl ester particles of one micron diameter at a constant temperature (4°C) and in dimethyl sulfoxide/ethanol:</li><li>.. Figure 4 is a graph showing iodipamide ethyl ester particle size as a function of temperature at a constant ratio of infusion rate of aqueous precipitating liquid to [stir rate (rpm) x volume of organic solution];</li><li>Figure 5 is a graph demonstrating the effect on particle size of varying the infusion rate of aqueous precipitating liquid at constant temperature and stirring rate . of an iodipamide ethyl ester solution; and</li><li>Figure 6 is a schematic diagram of preferred steps in the inventive method.</li></ul>

DETAILED DESCRIPTION OF THE INVENTION

0023This invention concerns the preparation of water-insoluble compounds as uniform particles of a predetermined size. The particles are formed by a carefully controlled precipitation of the compound into an aqueous phase from an organic solvent in which the compound is soluble.

0024The physical chemical principles thought to be involved in this invention are demonstrated in figures 1 and 2. Figure 1 shows that the free energy of the system is higher when the compound is dissolved in the organic solvent than when the compound exists in the particulate or crystalline state. During precipitation the compound will naturally convert to the crystalline form--the lowest free energy state--unless it is trapped in the metastable particulate form, a condition where its free energy is intermediate between the solution and the crystalline phases. When properly practiced, this invention enables the trapping of a compound in the metastable particle'state, precluding transformation to the crystalline state.

0025The size distribution of particles formed during precipitation can be correlated with the time interval between onset and completion of precipitation. As shown in Figure 2, a very short time interval results in the production of uniformly sized particles (A), while a very-long time interval results in a broad particle size distribution (B). Intermediate conditions produce intermediate particle size distributions.

0026An important parameter for utilization of this invention is the aqueous solubility of the compound. The invention requires the use of solid organic compounds having essentially little aqueous solubility. We have found that compounds which have a water-solubility of less than one part in ten thousand are ideally suited for this technology. Compounds which are more water-soluble can be used with this invention; however,, the higher the solubility the greater the probability that some of the compound will dissolve in the aqueous phase and transform to the more stable crystalline state. Also redissolution in the aqueous phase can lead to a broadening of the particle size distribution. For these reasons, we prefer compounds having a water-solubility of less than one part in ten thousand.

0027In order to make particles of a uniform and predetermined size having a solubility of less than one part per ten thousand, a solution of the solid organic compound'in a suitable organic solvent is prepared. The solution may be diluted with a non-solvent that does not cause the drug or other compound to precipitate. An aqueous precipitating liquid is also prepared, preferably with a surfactant, in sufficient quantity to both precipitate the drug or other compound and stabilize the resulting suspension of particles of the compound against aggregation. Water may be used alone as the precipitating liquid when compounds which do not aggregate are used. The aqueous solution is infused into the organic solution under carefully controlled conditions, including: the rate of stirring of the organic solution, the rate of infusion of the aqueous solution, the volume of the organic solution and the temperature of the solutions and the suspension.

0028In investigations of varying parameters to adjust for particle size, three usable relationships were discovered: (1) diluting the solution with more of the non-solvent produces larger particles, and diluting with less of the non-solvent produces smaller particles; (2) higher temperatures of the solution during precipitation produce larger particles, and lower temperatures of the solution during precipitation produce smaller particles; and (3) at a given stirring rate of the organic solution, faster infusion rates of aqueous solution produce smaller particles while slower infusion rates produce larger particles.

0029When the precipitation is complete, the uniformly sized particles are separated from the liquid and washed to remove the organic solvent. In most cases, the particles should be separated from the liquid quickly to prevent transformation to a crystalline form.

0030Compounds that are used in the invention-are solid organic materials, including organometallic compounds, that have a solubility in water of preferably less than one part per ten.thousand. Otherwise the specific compound and its purpose.are less important to the way the invention works.

0031The first step is to prepare a solution of the compound of interest in an organic solvent suitable for that compound. This can occur as the compound is synthesized as a dissolved solid, or it can be done by simply dissolving ths compound in the solvent of choice.

0032The solvent is chosen to suit the compound. For example, dimethylformamide (DMF) is a solvent for iothalamate ethyl ester (IEE) and iosefamate ethyl ester (IFE), and dimethylsulfoxide (DMSO) is a solvent for iodipamide ethyl ester (IDE) and IEE. Any satisfactory solvent for the compound that is miscible with water can be used.

0033The next step is to dilute the solution with a non-solvent that does not cause the compound to precipitate. The non-solvent causes greater dispersion of the dissolved molecules of the compound in the liquid phase. Greater dilution of the solution with non-solvent produces larger particles, and less dilution of the solution with non-solvent produces smaller particles.

0034The non-solvent should not precipitate the compound when it is added to the solution. Non-solvents in which the compound is slightly more soluble than in water are preferred. Lower aliphatic alcohols, such as ethanol, are effective non-solvents for solutions of IDE and IEE in DMSO. For the ethyl esters of triiodobenzoic acid, proportions of non-solvent to solvent at a ratio of 2 or more can produce 1 to 3 micron sized particles (depending on other parameters); and ratios of less than 2 can produce sub-micron particles, at least as applied to DMSO solutions diluted with ethanol.

0035To precipitate the compound from-the solution in a desired particle size, an aqueous solution of a surfactant is prepared in sufficient quantity to effect complete precipitation of the compound and to stabilize the resulting suspension of particles of the compound against aggregation. The surfactant provides the stabilization against aggregation. and the water is the precipitating agent. Presence of extra surfactant is advisable to ensure stabilization so that precipitated particles suspended in liquid do not aggregate, forming particles of an improperly large size. While surfactants are used in most cases, some compounds appear to form stable, substantially non-aggregated particles without the use of surfactants. Examples of such non-aggregrating compounds are certain Heparin complexes.

0036It is thought that particles with relatively high surface charge are less likely to require surfactant in the aqueous precipitating solution. The surface charge of a particle is sometimes referred to as its zeta potential, a measurement of charge which falls off with distance. There may be a threshold zeta potential above which no surfactant is needed, but below which, surfactant is needed to keep the precipitating particles from aggregating. The zeta potential is directly correlated with the polarity or net charge of an organic compound. Thus, the need for surfactant in the aqueous precipitating solution may be predicted from the extent of the charge or polarity of the organic compound employed in the method of the invention. For example, heparin comlexes are highly charged, and form stable non-aggregated particles when precipitated with water.

0037Generally, such a theory notwithstanding, empirical methods will suffice; that is, a precipitation may first be performed with water, and if aggregation occurs, then a precipitation in the presence of surfactant is indicated. Surfactants are chosen for their compatibility with the compound and their ability to stabilize a suspension of compound particles. For work with IEE and IDE drugs, a solution of 5% polyvinyl pyrrolidone (C-30), 0.1% polyvinyl pyrrolidone (C-15), or 0.1% human serum albumin is preferred. Also 0.1% Pluronic F-68, [Poloxamer 188, a poly(oxyethylene- co-oxypropylene) polymer], a 0.33% gelatin, 0.33% gelatin plus 0.6% Hetastarch, 0.33% gelatin plus 0.002% propylene glycol, and 0.33% gelatin plus 2% sucrose, or other surfacants known to one skilled in the art can be used.

0038To precipitate compound particles in the desired sizes, the aqueous solution and the organic solution are combined under controlled conditions of temperature, ratio of infusion rate to stirring rate, and the proportion of non-solvent to solvent in the dispersed solution.

0039The precipitation of the compound occurs exothermically, heating the organic solution and the resulting suspension. The temperature of the solution and resulting suspension is controlled to achieve the particle size of precipitate that is desired. Higher solution temperatures during precipitation produce larger particles, and lower solution temperatures during precipitation produce smaller particles.

0040Also, faster infusion rates at constant stirring rate of organic solution produce smaller particles, and slower infusion rates produce larger particles.

0041Figures three to five show the effects on particle size.of varying parameters during precipitation of IDE from a DMSO solution diluted with 1 part'solution to 2 parts ethanol using an aqueous solution of 5% polyvinyl pyrrolidone at different infusion rates and temperatures.

0042. FIG. 3 shows that as the volume and stirring rate of the organic compound iodipamide ethyl ester and dimethyl sulfoxide/ethanol solution are increased, the infusion rate of aqueous surfactant solution must be increased proportionally as defined by: infusion rate (ml/min.) = 23 + 0.14 [volume (liters) x stir rate (r.p.m.)] to produce particles of 1 micron diameter at 4°c.

0043FIG. 4 shows that at a constant ratio of infusion rate to [stir rate x volume], increased precipitation temperature produces larger particles.

0044FIG. 5 plots 3 points from the 20°C temperature line of FIG. 3 for rate of infusion of the precipitation liquid into the organic solution to approximate the curve by which larger particles are formed from slower injection rates, showing that at a constant ratio of temperature to [stir rate x volume], particle size is inversely related to the rate of infusion of the precipitating liquid.

0045When FIGS. 3-5 are considered together, they show clearly that higher temperatures and slower mixing rates produce larger particles, and lower temperatures and faster mixing rates produce smaller particles. Another parameter that can be varied to affect particle size is the amount of dilution of the solution before precipitation occurs.

0046When the precipitation is complete, extra aqueous . surfactant solution can be added to further stabilize the suspended particles against agglomeration. The extra solution can be added at a rapid rate, since essentially all the compound is now precipitated in uniformly sized particles. The precipitated particles are promptly separated from the organic solvents to prevent redissolving and reprecipitation of particles at undesirable sizes. Centrifuging is a preferred way to perform the separation. Other methods, including membrane filtration, reverse osmosis, and others known to persons skilled in the art may also be used to remove undesired substances. Promptly after separating the particles t from the organic liquid, the particles are washed or rinsed with normal saline solution to remove solvent and excess surfactant.

0047The method of the invention is illustrated by the following examples which, however, do not limit the invention as described above and set forth in the claims.

0048Examples 1 to 19 are presented in Table I. The solid organic compound was dissolved in the organic solvent and then diluted (except where indicated) by the non-solvent. The aqueous precipitating liquid was then infused through a needle at the given rate into the solution, at the given temperature and while stirring at the given stirring rate. The size of the particles obtained is shown for each example. <tables id="tabl0001" num="0001"><img file="EP0169618A2_D0001.tif" /></tables><tables id="tabl0002" num="0002"><img file="EP0169618A2_D0002.tif" /></tables><tables id="tabl0003" num="0003"><img file="EP0169618A2_D0003.tif" /></tables><tables id="tabl0004" num="0004"><img file="EP0169618A2_D0004.tif" /></tables><tables id="tabl0005" num="0005"><img file="EP0169618A2_D0005.tif" /></tables><tables id="tabl0006" num="0006"><img file="EP0169618A2_D0006.tif" /></tables><tables id="tabl0007" num="0007"><img file="EP0169618A2_D0007.tif" /></tables><tables id="tabl0008" num="0008"><img file="EP0169618A2_D0008.tif" /></tables><tables id="tabl0009" num="0009"><img file="EP0169618A2_D0009.tif" /></tables><tables id="tabl0010" num="0010"><img file="EP0169618A2_D0010.tif" /></tables>

0049Examples 1 to 19 show how the process can be used to produce aqueous dispersions of a wide variety of compounds that have low aqueous solubility and for which particle size can be controlled with substantial precision and predictability. Conditions would be varied from compound to compound according to the invention in order to optimize results. -This may in some cases include chemical modification of the compound to achieve the desired solubility.

0050Because of the range of examples presented above, it is reasonable to one skilled in the art, that numerous other compounds would be expected to behave in similar fashion.

0051Example 20 is also presented in Table I. This example should be performed in the same manner as examples 1 to 19, and would make particles of the listed compounds within the scope of the invention.

0052Examples .21 to 28 are presented in Table II. In each example, the given quantity of iodipamide ethyl ester was dissolved in the given volume of-dimethyl sulfoxide,-then diluted with the given volume of ethanol. The aqueous precipitating liquid was prepared from polyvinylpyrrolidone then infused at the given infusion rate through a needle with the given gauge into the solution while the solution was stirred at the given stir rate. The precipitation was carried out in the given vessel at the given temperature. After precipitation, the given amount of saline was added to further stabilize the dispersion. In each example, the mean particle diameter was about 1.0 micron and substantially uniform. <tables id="tabl0011" num="0011"><img file="EP0169618A2_D0011.tif" /></tables><tables id="tabl0012" num="0012"><img file="EP0169618A2_D0012.tif" /></tables><tables id="tabl0013" num="0013"><img file="EP0169618A2_D0013.tif" /></tables>

PREPARATION OF IODIPAMIDE ETHYL ESTER PARTICLES FOR ADMINISTRATION TO A PATIENT.

0053Particles of iodipamide ethyl ester (IDE) with a size of about 1 micron may be prepared for administration to a patient. IDE is the water-insoluble ethyl ester of iodipamide, a water-soluble radiopaque compound used clinically for radiographic examination of the gallbladder. The synthesis of iodipamide ethyl ester is known in the art (for example, esterification by alcohol and acid or by a Schotten-Bauman reaction).

0054IDE is only minimally soluble in water (10^-5 M) and can be precipitated easily from the dimethyl sulfoxide (DMSO)/ethanol solvent mixture. However, the simple addition of water to this solution results in IDE particles with extremely rough contours; these particles vary in size from less than one micron to greater than.300 microns in diameter. In light of the problems that rough contours could damage vascular endothelial cells and promote aggregation, and that large particles could create pulmonary emboli, the method of this invention provides a more refined procedure for controlling particle size and shape.

0055Particle Precipitation Procedure. Physical methods for modifying and controlling particle size, such as ball milling, grinding or sonication result in preparations with a very broad range of particle diameters. These methods are commonly used to eliminate large particles (greater than 4-5 microns) which could embolize in the pulmonary capillary bed, but generally some particles of submicron size are also produced; these very small particles have been shown to be more toxic than 1-2 micron particles, possibly due to increased protein binding resulting from the much larger surface area inherent with particles of smaller diameters, or possibly because of excessive uptake by bone marrow cells.

0056A chemical precipitation procedure for producing particles of a given size was developed to avoid these- problems. By adding an aqueous solution of polyvinyl pyrrolidone, at controlled rates and temperatures, to IDE dissolved in a dimethyl sulfoxide/ethanol solvent, apparently spherical, amorphous particles can be produced with an extremely narrow size distribution. For a particle preparation with a mean diameter of 1 micron, the total range of particle diameters is 0.4 to 2.0 microns with 90 per cent of the particles ranging in size between 0.5 and 1.5 microns, as determined by microscopy.

0057By carefully controlling precipitation parameters, particle preparations demonstrating different mean diameters, but with a similarly small range of diameters, can be produced.

0058The IDE particles produced using this methodology are stable in whole blood with little apparent tendency toward aggregation. When suspended in whole blood, there is essentially no tendency for one micron IDE particles to aggregate with themselves or with formed elements of bleed. The IDE particles have smooth contours.