Pharmaceutical liquids, compounding solutions

Yet, there are still many hurdles that must be overcome before these substances can be put to widespread use. Because ionic liquids boil at high temperatures, conventional methods of separating reaction products from solution cannot be used. Pharmaceutical manufacturing processes, for instance, often involve the process of distillation. The higher temperatures required to distill using ionic liquids (as opposed to organic liquids) would decompose many of the desired pharmaceutical compounds. 

Inhalation and direct skin contact are the most common routes of chemical exposure. The greatest exposure risk in handling potent compounds in an analytical laboratory therefore occurs when handling solid materials due to the potential to generate and inhale airborne dust particles of the compound. Once the potent material has been placed into solution, the airborne exposure risk is reduced and solutions of potent compounds may be handled in a manner similar to other nonpotent pharmaceutical compounds, assuming good laboratory practices are followed. Caution should be taken not to aerosolize the solutions since this could create an inhalation hazard. In addition, any sample solution spills should be adequately cleaned to prevent powder deposits of the compound from forming, which could potentially become airborne after the liquid has dried. 

Optical chirality of molecules is a characteristic measure of stereo-chemical property of biological, pharmaceutical, and metal coordination compounds. Choral structures of amino acids, proteins, DNAs, and various drugs in solutions have been determined from the measurement of circular dichroism (CD). However, small amount of molecules at the liquid-liquid interfaces has never been measured before CLM/CD method [19] and SHG/CD method have been reported [20],... 

Ketamine is a compound with a molecular structure similar to that of phencyclidine (Figure 4.2). The pharmaceutical versions of ketamine are clear, colorless liquids available in varying concentrations of 10,50, and 100 milligram/milliliter solutions (Figure 4.3). Many recreational users inject this liquid intramuscularly or intravenously. It is the liquid formulation that is used as a date rape drug. Liquid ketamine, which is clear and colorless, can easily be slipped into a drink without being detected. 

OMD offers major advantages in comparison with the conventional thermal concentration techniques. The low temperature employed can help avoid chemical or enzymatic reactions associated with heat treatment [85] and prevent degradation of flavor, color, and loss of volatile aroma [38]. The low-operating pressure (atmospheric pressure) results in low investment costs, low risks of fouling, and low limits on compactive strength of the membrane. Since the separation is based on vapor-liquid equilibrium, only volatile compounds which can permeate the membrane and the nonvolatile solutes such as ions, sugars, macromolecules, cells, and colloids are totally retained in the feed. These factors make OMD an attractive alternative to traditional thermal routes currently used for concentration of liquid foods or aqueous solutions of thermally labile pharmaceutical products and biologicals [86]. 

The solubility measure describes the concentration reached in solution, when a pure phase of the material is allowed to dissolve in the solvent for a defined period of time, at a defined temperature (and pressure). Most often for pharmaceutical purposes, the pure phase is a solid, ideally a crystalline solid, and the liquid is water or a buffered aqueous solution, at a controlled temperature (often 25 or 37 °C) and ambient pressure. The purity of the solid can have a large effect on measured solubility. Solubility can be measured in water or in pH-controlled buffers. In water, the extent of solubility for ionizable compounds will depend upon the p fCa values and the nature of the counterion. In pH-controlled aqueous buffered solution, at equilibrium, the solubility will depend upon the compound s intrinsic solubility, its plQ, and the ionic strength. It may also depend upon the relative solubility of the initial added compound and the solubility of the salt formed by the compound with the buffer salts, with which the solid may equilibrate. In any buffer or solvent system, the measured solubility may depend on the time of sampling, as solubility kinetics... 

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