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Biomedical subjects

J T Rubino

Publications and source records attributed to J T Rubino.

16 recordsLinked to original sources

Photoinduced particulate matter in a parenteral formulation for bisnafide, an experimental antitumor agent.

This paper assesses the cause of particulate formation in vials of the experimental antitumor agent bisnafide and investigates pharmaceutical techniques to reduce the number of particulates in the product. Solution preparation and particulate isolation were performed under Class 100 laminar air flow. Reversed-phase HPLC and infrared microscopy were used to characterize drug and isolated particulate matter, whereas a Hiac particle counter was used to quantify the particulate matter. Particulate matter was observed following agitation of the drug solutions and was found to be associated with specific lots of drug substance. HPLC of the isolated particulate matter indicated that the particulates consisted largely of bisnafide and impurities that were identified as the products of photodegradation, confirmed to be the result of the photolytic cleavage of bisnafide to form a poorly soluble aldehyde. The aldehyde may, in turn, interact with bisnafide molecules to form the particulate matter as suggested by the observed pH-dependent reversibility of the particulate phenomenon. The particulate matter could be reduced by protecting solutions of bisnafide from light during chemical synthesis and production of the dosage form and, alternatively, by reducing the solution pH to 3.0 or less, addition of surfactants below their critical micelle concentration, and removal of impurities by froth flotation of the bisnafide solutions.

Aldehydes↗

Validation of cleaning procedures for highly potent drugs. II. Bisnafide.

The objective of this work was the development and validation of procedures designed to clean glass and stainless steel surfaces after exposure to the experimental anticancer drug, bisnafide. The cleaning procedures, using 5% acetic acid water, Alconox, and water, were validated using a wipe test and an HPLC method developed to quantitate low levels of bisnafide. The procedure developed for cleaning stainless steel is more stringent than that for glass because of the apparent greater affinity of bisnafide for stainless steel. The HPLC method is shown to be linear and reproducible (RSD 4.4% or less), with a detection limit of 4 ng/ml. Recoveries of 95.1, 83.5, and 70.0% were obtained from the wipe pads, glass plates, and stainless steel plates, respectively, at levels of approximately 0.7-1.7 ng/cm2. The cleaning procedures are shown to clean glass and stainless steel plates to less than 0.19 and 0.33 ng bisnafide/cm2, respectively. These results further demonstrate the need to fully characterize the recovery of drugs from surfaces and swabs in order to properly validate cleaning procedures. In addition, they demonstrate the potential need to develop surface-specific cleaning procedures.

Antineoplastic Agents↗

Validation of cleaning procedures for highly potent drugs. I. Losoxantrone.

The validation of a procedure designed to clean glass and stainless steel surfaces after exposure to the experimental anticancer drug losoxantrone is described. The cleaning procedure, using water and hypochlorite bleach, was validated using a wipe test and a high-performance liquid chromatography (HPLC) method developed to quantitate low levels of losoxantrone. The HPLC method is shown to be linear and reproducible (relative standard deviation (RSD): 7.1% or less), with a detection limit of 2 ng/ml. Recoveries of 71.0%, 50.1%, and 57.6% were reproducibly obtained from the wipe pads, glass plates, and stainless steel plates, respectively, at levels of 70-140 ng per 100 cm2. The cleaning procedure is shown to clean glass and stainless steel plates to less than 20 ng and 17 ng losoxantrone per 100 cm2, respectively. These results demonstrate the need to fully characterize the recovery of drugs from surfaces and swabs in order to properly validate cleaning procedures.

Anthraquinones↗

Influence of solute structure on deviations from the log-linear solubility equation in propylene glycol:water mixtures.

The solubilities of the methyl, ethyl, propyl, and butyl esters of p-hydroxy- and p-aminobenzoates have been determined in propylene glycol:water mixtures. The log of the observed solubility data in propylene glycol:water mixtures was examined for deviations from the following equation: In Xi = f In (Xc) + (1 - f) In (Xw), where Xi is the calculated mole fractional solubility of the solute, f is the volume fraction of cosolvent, Xc is the observed mole fractional solubility in the neat cosolvent, and Xw is the solubility in water. In each case, the deviations from the predicted solubilities demonstrated a characteristic pattern. Positive deviations were observed at high volume fractions of cosolvent, while negative deviations were observed at low volume fractions. The magnitude of the deviations at low volume fractions of cosolvent was related to the carbon chain length within each group of esters. A similar phenomenon was not observed at high volume fractions of cosolvent; however, the magnitude of the deviations was dependent on the nature of the polar group on the ester. The data are interpreted in terms of the possible effects of solvent structure on the solubility of the solutes.

Benzoates↗

Solubilities and solid state properties of the sodium salts of drugs.

The solubilities in water of a number of sodium salts of weakly acidic drugs were determined. The compounds examined included barbiturates, sulfonamides, and hydantoins. When the logarithm of the aqueous solubilities of the salts were plotted against their melting points, an inverse relationship was observed; however, a good correlation was not immediately apparent. Further studies were conducted on the solid phases of the drugs after equilibration with water, using calorimetric, spectrophotometric, and gravimetric methods. In many cases, hydrate formation was evident and, for some compounds, the stoichiometric amount of water in the crystal was different before and after equilibration with water. Multivariate analysis of the data indicated that the logarithms of the molar solubilities were inversely related to both the melting points and the stoichiometric amounts of water in the crystal hydrates, but were unrelated to the polarity of the corresponding acid forms of the drugs. Therefore, for the sodium salts of these drugs, the solubility is primarily controlled by the properties of the solid phase which exists in equilibrium with the solution phase.

Calorimetry↗

Cosolvency and deviations from log-linear solubilization.

The solubilities of three nonpolar drugs, phenytoin, diazepam, and benzocaine, have been measured in 14 cosolvent-water binary mixtures. The observed solubilities were examined for deviations from solubilities calculated by the equation log Sm = f log Sc + (1 - f) log Sw, where Sm is the solubility of the drug in the cosolvent-water mixture, Sc is the solubility of the drug in neat cosolvent, f is the volume fraction of cosolvent, and Sw is the solubility of the drug in water. When presented graphically, the patterns of the deviations were similar for all three drugs in mixtures of amphiprotic cosolvents (glycols, polyols, and alcohols) and water as well as nonpolar, aprotic cosolvents (dioxane, triglyme, dimethyl isosorbide) and water. The deviations were positive for phenytoin and benzocaine but negative for diazepam in mixtures of dipolar, aprotic cosolvents (dimethylsulfoxide, dimethylformamide, and dimethylacetamide) and water. The source of the deviations could not consistently be attributed to physical properties of the cosolvent-water mixtures or to alterations in the solute crystal. Similarities between the results of this study and those of previous investigations suggest that changes in the structure of the solvent play a role in the deviations from the expected solubilities.

Benzocaine↗

Cosolvency and cosolvent polarity.

The solubilities of three poorly soluble drugs, phenytoin, benzocaine, and diazepam, in cosolvent-water mixtures have been previously shown to be approximated by the log-linear solubility equation; log (Sm/Sw) = sigma f, where Sm and Sw represent the solubilities of the drug in the solvent mixture and water, respectively, f is the volume fraction of cosolvent, and sigma is the slope of a plot of log (Sm/Sw) vs f. In this study, the slopes, sigma, of the solubility plots were related to indexes of cosolvent polarity including the dielectric constant, solubility parameter, surface tension, interfacial tension, and octanol-water partition coefficient. Those polarity indexes that reflect the cohesive properties of the solvents such as the solubility parameter and interfacial tension resulted in the highest correlations with the slope, sigma. The hydrogen bonding ability of the neat cosolvent, expressed as the density of proton donating groups (HBD) or acceptor groups (HBA), was also found to be highly correlated with sigma. Additional relationships derived from theories involving solubility parameters and interfacial tension provide improved correlations between the cosolvent polarity and sigma. These results and analysis provide the basis for the estimation from physicochemical parameters of the appropriate type and amount of cosolvent needed to solubilize nonpolar drugs.

Benzocaine↗

Effects of solvent polarity on the acid dissociation constants of benzoic acids.

The pKa values of benzoic acid, p-methylbenzoic, and p-aminobenzoic acid (PABA) were determined by potentiometric titration in mixtures of 0-0.5 volume fractions of various cosolvents and water. The differences between the aqueous and semiaqueous pKa values were similar for the three solutes at a particular cosolvent-water mixture for most of the cosolvents studied. The largest differences occurred in the dimethyl sulfoxide (Me2SO)-water system, where the pKa changes were larger for PABA than the other two solutes. The data are analyzed by a consideration of both electrostatic and nonelectrostatic medium effects. The electrostatic medium effect was calculated from the Born Equation while any residual pKa change was attributed to nonelectrostatic medium effects. The residual effects were found to correlate well with indexes of solvent hydrogen bond acceptor ability such as HBA and beta-values. These results provide a rationale for the use of two solvent polarity indexes for more accurate estimates of pKa values of weak electrolytes in semiaqueous solvent systems. Analysis of solubility data of the salt and acid forms of PABA and benzoic acid in ethanol-water and Me2SO-water mixtures suggests that the higher activity of the anionic form of PABA in Me2SO-water mixtures is primarily responsible for the large pKa changes observed for that solute.

Benzoates↗

Solubilization by cosolvents I: organic solutes in propylene glycol-water mixtures.

An equation describing solubilization in aqueous systems by cosolvents was developed by treating a mixed solvent as a linear combination of its components. This equation can successfully explain both the exponential increases and the exponential decreases in aqueous solubility that are frequently observed with the addition of cosolvent. It also provides a means of estimating to what extent a particular drug can be solubilized and how much cosolvent would be required to accomplish a particular degree of solubilization.

Chemical Phenomena↗

The influence of charged lipids on the flocculation and coalescence of oil-in-water emulsions. I: Kinetic assessment of emulsion stability.

The influence of various negatively charged lipids on the stability of phospholipid stabilized oil-in-water emulsions in the presence of varying concentrations of calcium chloride was examined by a measurement of the changes in the turbidity of the emulsion over time. The data were described well by the following equation: (Ai - A) = (Ai - A0) exp(-kt) where Ai is the maximum spectrophotometric absorbance achieved in the system, A is the absorbance at time t, A0 is the absorbance at the start of the experiment and k is the flocculation or coalescence rate constant. Plots of k and Ai/A0 vs. concentration of Ca++ provided an indication of the rate and extent of emulsion flocculation/coalescence, respectively. The sodium salts of phosphatidic acid (SPA) and oleic acid (SO) increased the critical flocculation concentration of calcium while sodium phosphatidylinositol (SPI) and sodium phosphatidylserine (SPS) had no effect on the critical flocculation concentration compared to the control emulsion. The addition of all lipid salts increased the rate of flocculation compared to the control emulsion, however, emulsions containing SPI demonstrated the highest values of k. In contrast, emulsions containing SO coalesced to the largest extent, as indicated by large values of Ai/A0. Systems containing charged phosphatides regained some stability in higher concentrations of Ca++ while those containing oleate were comparatively more unstable up to 20 mM Ca++. Based upon the results of the present studies, it appears that phosphatidic acid is the most important fraction of the anionic phosphatides in stabilizing an emulsion in the presence of calcium ion.(ABSTRACT TRUNCATED AT 250 WORDS)

Drug Stability↗

The influence of charged lipids on the flocculation and coalescence of oil-in-water emulsions. II: Electrophoretic properties and monolayer film studies.

The influence of calcium ions on the electrophoretic properties of phospholipid stabilized emulsions containing various quantities of the sodium salts of oleic acid (SO), phosphatidic acid (SPA), phosphatidylinositol (SPI), and phosphatidylserine (SPS) was examined. The critical flocculation concentration of calcium corresponded to a critical zeta potential in all but one of the systems. Systems of approximately equal zeta potential in 0 mM Ca++ had different zeta potentials in dilute solutions of Ca++. A comparison of emulsions of similar polydispersity suggests that these differences may be largely related to differences in particle size and surface area of the emulsions. The influence of Ca++ on the monolayer properties of mixed films containing phosphatidylcholine (PC) with either SPA or SO was also examined at the air-water interface. Films containing PC with SPA were more expanded on a subphase containing calcium compared to a subphase with no calcium. In addition, the compression of films containing PC with SO demonstrated two collapse pressures while SPA was relatively more miscible in the film. This suggests that phase separation of interfacial lipids occurs more easily in systems containing PC and SO. These results may help to explain differences in the flocculation and coalescence of emulsions stabilized by lipid films of different composition.

Electrophoresis↗

Dynamic compatibility testing of DMP 840, an experimental antitumor agent.

The purpose of this study is to evaluate the potential for DMP 840, a novel experimental antitumor agent, to precipitate during injection or dilution with infusion solutions. The influence of predilution of the drug solution before injection and addition of buffers to the drug vehicle were also investigated. The compatibility of normal saline solution, pH 7.4 phosphate buffers, and human plasma with DMP 840 was examined in vitro under both static conditions and dynamic flow. The combination of DMP 840 solutions with normal saline solution resulted in conversion of the drug to an insoluble dihydrochloride salt. Under conditions of dynamic flow, precipitation, accompanied by large changes in turbidity, occurred at relatively high concentrations of the drug in the injection solution. Dilution of the injection solution below 2 mg/mL or slow injection avoided precipitation. As was the case with the normal saline system, turbidity changes after injection into protein-phosphate buffer (PPB) were dependent on the initial concentration of DMP 840 solution as well as the rate of administration. In addition, the maximum injection rate at which complete miscibility occurred increased exponentially as the drug injection solution was made more dilute. Buffering the DMP 840 injection solution with acetate buffer improved the miscibility of DMP 840 with PPB, which indicated that the turbidity increases were most likely due to conversion of the drug to its insoluble free base form. The observed effects of the buffer on the turbidity response agreed qualitatively with predictions from a graphical approach that considers the effects of dilution and pH changes on drug solubility. Despite these observations, no evidence for the formation of a solid precipitate could be found after injection of the unbuffered drug solution into PPB. Further investigation indicated that the presence of albumin in the PPB prevented the formation of a solid phase during injection. Likewise, fresh human plasma, spiked with 1 and 2 mg/mL solutions of DMP 840, showed no evidence for the formation of a solid precipitate.

Antineoplastic Agents↗