Abstract: A method and device are disclosed for transferring information from cinema film at a first speed to broadcast quality video signals at a second and different, predetermined speed which may be greater or less than the first speed in a telecine containing a capstan and an internal frame store. The device comprises (1) a mechanism for determining rotational phase and velocity of the capstan, and (2) a servo motor driven at a rate outside the frame store given range, including means to adjust the linear film rate to an integer multiple/submultiple of the framestore pulse rate.

Abstract: A releasable coupling connector apparatus for catheter applications is provided wherein the connector is partially filled wtih anti-infective solution during manufacture and capped so that a patient or medical technician does not have the task of opening the fluid pathway and introducing the anti-infective solution at point of use into the connector apparatus. The connector apparatus being partially filled with anti-infective solution and capped during manufacture is further sterilized by Gamma radiation in order to eliminate any organism resistant to the anti-infective solution. The releasable coupling connector apparatus provides the first practical double seal connector means wherein a double seal connector defining dual sterilant liquid containing chambers for use with catheter applications and particularly with CAPD whereby sterilization is assuredly and easily achieved by an impaired, unskilled patient even under adverse conditions.

Abstract: Specifically, the present invention relates to processes for preparing delayed action galenic forms. The process is characterized in that the application solutions of excipients, coatings and active constituents are adjusted to a desired pH. The independence of the rate of dissolution of a controlled release or sustained action oral pharmaceutical form is increased by admixing a pH adjusting agent with every application solution of medicament, excipeint or coating, throughout the course of formulation of the pharmaceutical form.

Abstract: A controlled release powder containing discrete micro-particles for use in edible, pharmaceutical and other controlled release compositions is disclosed. The micro-particles have an average size in the range of from 0.1 to 125 .mu.m. Each of the micro-particles is in the form of a micromatrix of an active ingredient uniformly distributed in at least one non-toxic polymer. The micro-particles have a predetermined release of active ingredient when the dissolution rate thereof is measured according to the Paddle Method of U.S. Pharmacopoeia XX at 37.degree. C. and 75 r.p.m.

Abstract: Processes for producing aloe extracts including the separation of the leaves of the aloe plant into distinct portions. In particular, a first process is described for producing an aloe extract which is substantially free of anthraquinone-rich yellow sap and a second process is described for extracting the active chemical substance in the aloe plant.The active chemical substance in the aloe plant is extracted from aloe leaves and its characteristic properties are described.

Abstract: A sustained absorption propranolol-containing pellet for oral administration comprises a core of propranolol or a pharmaceutically acceptable salt thereof and an organic acid embedded in a polymeric material in a multi-layer arrangement and an outer membrane which permits release of the propranolol at a controlled rate in an aqueous medium. The pellet has a dissolution rate in vitro in an aqueous medium, which when measured in a basket assembly according to U.S. Pharmacopoeia XX at 37.degree. C. and 75 r.p.m., is not more than 15% of the total propranol after 2 hours of measurement in a buffer solution at pH 7.5. Not more than 30% of the total propranolol is released after a total of 4 hours of measurement and not more than 63% of the total propranolol is released after a total of 6 hours.

Abstract: A diltiazem pellet formulation for oral administration comprises a core of diltiazem or a pharmaceutically acceptable salt thereof in association with an organic acid, and a multi-layer membrane surrounding the core and containing a major proportion of a pharmaceutically acceptable film-forming, water insoluble synthetic polymer and a minor proportion of a pharmaceutically acceptable film-forming, water soluble synthetic polymer. The number of layers in the membrane and the ratio of the water soluble to water insoluble polymer being effective to permit release of the diltiazem from the pellet at a rate allowing controlled absorption thereof over a twenty four hour period following oral administration.

Abstract: The present invention relates to medicaments with a high degree of dissolution rate and solubility. These medicaments are characterized in that they are in amorphous form produced by spraying in the presence of a stabilizer and of an agent inhibiting the formation of crystals.

Abstract: A new and useful indigo-dyeable polyester is disclosed, and process for making same, for which a suitable polyester has had applied to its surface an amount of a suitable indigo dye retaining compound effective to provide said polyester with indigo fastness properties similar to cotton. The new indigo dyeable polyester may be employed in the manufacture of a staple material blended with cotton in predetermined amounts depending on the end use desired, e.g., 50:50 by weight for cotton denims (e.g., jeans). Preferable indigo dye retaining compounds comprise monomers dioleylamine and dicocoamine. Other suitable indigo dye retaining monomers are disclosed, inter alia, having the formula: ##STR1## wherein R.sub.1 is alkyl or alkenyl of about 10-18 carbons; R.sub.2 is alkyl, alkylaryl, or alkenyl of about 8-18 carbons, R--CH.sub.2 --NO.sub.2, R--CH.dbd.NH, where R is alkyl or alkenyl from one to eighteen carbons; and R.sub.3 is hydrogen or alkyl from one to about twelve carbons.

Abstract: A new and useful composition of matter, solid at room temperature, is disclosed, comprising: (1) an effective amount of a suitable nucleating agent substantially uniformly dispersed in (2) a suitable pressure-sensitive adhesive for encapsulating a temperature-sensitive solid mixture having a given nucleation efficiency and which melts at a predetermined temperature, whereby the suitable nucleating agent is (a) inert to both the pressure-sensitive adhesive and the temperature-sensitive solid mixture, and (b) capable of raising the nucleation efficiency of said solid mixture. The novel composition of matter overcomes the extreme super-cooling achieved by temperature-indicating compositions of matter in U.S. Pat. No. 4,232,552 (which change color with a change in phase) without the use of classical nucleating agents being employed in such temperature-indicating compositions of matter.

Abstract: A new and useful container is disclosed for storing "sharps", e.g., surgical needles or blades, comprising: (a) base means formed of a reusable and sterilizable material containing a source of magnetism; (b) collecting means for surgical needles or blades, said collecting means shaped to provide an interlocking fit with said base means; and (c) cover means with said collecting means to form an enclosure, said cover means capable of tight-fitting engagement with and placement over said collecting means to prevent said surgical needles or blades from escaping from said enclosure when said cover means is in tight-fitting engagement with said collecting means, said collecting means and said cover means attached to each other by hinge means, said collecting means being provided with locking means to lock said cover means with said collecting means when said cover means is in tight fitting engagement with said collecting means.

Abstract: Processes, reagents and test kits for the qualitative and/or quantitative determination of an immunochemically reactive component, in which one or more labelled components are used, that are obtained by direct or indirect coupling of such a component or components to particles of an aqueous dispersion of a hydrophobic dye or pigment, or of polymer nuclei coated with such a dye or pigment.During the reaction or after an adequate reaction time the nature and/or the quantity of the dye is determined in the test medium, or optionally after a separation of the bound and free labelled components in one of the fractions.

Abstract: A new and useful hydrophilic polyester fiber and process of making same are disclosed; the fiber has a stable pore system exhibiting a moisture pickup (regain) of at least about 2 percent by weight at 40.degree. C. and a relative humidity of 92%. Our experiments indicate that the proportion of moisture regain is attributable to capillary condensation in an amount of at least 25%. The hydrophilic properties are the result of a certain pore system within the fiber which enables capilliary condensation to occur significantly. The invention describes one way to accomplish this, namely by the addition of a predetermined amount of a suitable oxalato-complex to a suitable polyester mass. Most preferably, about 10% by weight K.sub.3 Al(C.sub.2 O.sub.4).sub.3 is added to the polyester mass.

Abstract: A new and useful process is disclosed for manufacturing a device for use in a bioprocess, comprising: (a) providing solid support means insoluble in water or organic solvent solutions; (b) coating said solid support means with water-based polymeric film means capable of applying one or more biomaterials; and (c) adsorbing or covalently bonding at least one functional biomaterial to said polymeric film means. The polymeric film means, for example, can be used to coat antigens, antibodies, haptens, enzymes, living bacteria, yeasts, etc. (i.e., biomaterials) to a glass (or other) support material, e.g., a glass tube, with surprising retention of the biomaterial's essential characteristic properties. The solid support means include but are not limited to those comprising glass, ceramics, metals, polymers and woods. The device of the invention is particularly useful in various immunoassays using a solid support for separation of phases.

Abstract: A method of blanking wherein an endless V-shaped groove of desired contour is formed on at least one of the top and bottom sides of a material sheet. The groove is shaped so that the external side thereof is at a right angle to the groove-cut surface of the sheet. A blank having the desired contour is then cut out of the sheet along the right-angled external side of the groove.

Abstract: Novel and stable compositions of matter are disclosed which change color sharply upon a transition from a liquid state to a solid state or from a solid state to a liquid state, which change of state is at substantially a predetermined temperature corresponding to a temperature to be measured.The constituents of the novel compositions of matter comprise:1. a solvent (I) consisting of a single substance or a mixture of substances and adapted to change from a solid state at substantially a predetermined temperature to a liquid state and2. an indicator system (II) consisting of one or more substances different from (I), characterized in that(a) (II) is soluble in (I) when the latter is in the liquid phase, and(b) (II) changes color visible to the naked eye when (I) passes from the solid to the liquid phase or from the liquid to the solid phase.Thermometers containing said stable compositions of matter are also disclosed.

Abstract: There is disclosed a sodium zirconium carbonate compound and the method of its preparation. The sodium zirconium carbonate compound is formed from a metastable aqueous solution comprising zirconium, sodium, sulfate, and carbonate ions.

Abstract: A new and useful process is disclosed for manufacturing a device for use in a bioprocess, comprising: (a) providing solid support means insoluble in water or organic solvent solutions; (b) coating said solid support means with organic-solvent based polymeric film means capable of applying one or more biomaterials; and (c) adsorbing or covalently bonding at least one functional biomaterial to said polymeric film means. The polymeric film means, for example, can be used to coat antigens, antibodies, haptens, enzymes, living bacteria, yeasts, etc. (i.e., biomaterials) to a glass (or other) support material, e.g., a glass tube, with surprising retention of the biomaterial's essential characteristic properties. The solid support means include but are not limited to those comprising glass, ceramics, metals, polymers and woods. The device of the invention is particularly useful in various immunoassays using a solid support for separation of phases.

Abstract: A new and useful all plastic disposable thermometer is disclosed, which dispenses with the prior art employment of an aluminum or other metal-based substrate. The novel thermometer can either be employed with opaque indicator means or with heat-sensitive compositions of matter that change color with a change in phase, such as those enumerated in copending application Ser. No. 946,935, filed Sept. 28, 1978, now U.S. Pat. No. 4,232,552.

Abstract: An improved steam sterilization indicator is provided. The indicator includes a fusible material in tablet form, deposited in an embossment in one end of a thin aluminum backing. A wicking strip is attached to the backing with one end of the strip being in close proximity to the fusible tablet. A clear plastic material covers the tablet and the strip and is adhered to the backing. The melting point of the fusible tablet is depressed in the presence of saturated steam. Upon melt, the material in the tablet is absorbed by the wicking strip, producing a color front to provide an indication of the integration of time and temperature in the presence of steam. Various amounts of a binder are used in the tablet to provide a device which may be adjusted to reflect the thermal death curves of various types of microorganisms. The cover and the wick are bonded to the backing by an acyclic adhesive which also affects the rate of the indicator.