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PubMed2006

Dissolution behavior and in vitro evaluation of sputtered hydroxyapatite films subject to a low temperature hydrothermal treatment.

Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as-sputtered films were hydrothermally recrystallized at 110 degrees C. In immersion tests, the as-sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 osteoblast-like cells on the as-sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3-E1 cells on the as-sputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as-sputtered film. After a 96-h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titanium substrate, and as-sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3-E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3-E1 cells on the as-sputtered films after a period of 24 h.

Animals↗
PubMed2005

Permeability of adhesive resin films.

The purpose of this study was to quantify the permeability of adhesive resin films to water by measuring convective flow across thin films. Cured resin films were prepared with the use of five commercially available adhesive resins and an experimental resin. Two types of resin films were prepared from solvated comonomer blends within each product; resin films made before or after evaporation of solvent (10 s of drying with air-syringe). The permeability of the resin films was measured 30 min or 24 h after polymerization by placing the films in a split-chamber device. Fluid filtration rate through the resin films was measured with the use of 20 cm of water pressure. Osmotically induced water movement was measured by applying hypertonic aqueous solutions of CaCl2 or HEMA to the resin films. The results showed that evaporation of solvent before polymerization reduced the permeability of adhesive resin films, compared to permeabilities obtained without solvent evaporation. The cured adhesive resin films were all permeable to water, but to varying degrees.

Adhesives↗
PubMed1986

Adhesion of hydroxypropyl cellulose films to low energy solid substrates.

The adhesion of hydroxypropyl cellulose (HPC) to well-defined solid substrates was measured as a function of dry film thickness. A well-controlled butt adhesion test, providing a constant slow rate of film detachment, was used to keep the viscoelastic contribution of the film to the adhesion measurement constant. Films were cast or sprayed from solution in either triply distilled water or absolute ethanol onto relatively smooth surfaces of poly(methyl methacrylate), poly(ethylene terephthalate), and polyethylene. A linear relationship of increasing adhesion with decreasing dry film thickness was obtained for thin films (less than 20-microns thick) on all three surfaces. An adhesion value, A0, determined by extrapolating the adhesion data to zero film thickness, was shown to be proportional to the calculated thermodynamic work of adhesion, Wa, at the film-substrate interface. No significant effect of the method of film preparation, cast or sprayed, on the adhesion measurement was noted. Adhesion for a given film thickness was greater for films prepared from solutions having a higher initial polymer concentration or when using ethanol as opposed to water as the solvent.

Adhesiveness↗
PubMed2005

Alkaline and enzymatic degradation of L-lactide copolymers, 1. Amorphous-made films of L-lactide copolymers with D-lactide, glycolide, and epsilon-caprolactone.

Films of poly(L-lactide) [i.e., poly(L-lactic acid) (PLLA)] and L-lactide copolymers with glycolide [P(LLA-GA)(81/19)], epsilon-caprolactone [P(LLA-CL)(82/18)], D-lactide [P(LLA-DLA)(95/5), (77/23), and (50/50)] were prepared and a comparative study on the effects of comonomer type and content on alkaline and proteinase K-catalyzed hydrolyses of the films was carried out. The hydrolyzed films were investigated using gravimetry (weight loss and water absorption), differential scanning calorimetry (DSC), polarimetry, and gel permeation chromatography (GPC). To exclude the effects of molecular weight and crystallinity on the hydrolysis, the films were prepared from polymers having similar molecular weights and made amorphous by melt-quenching. It was found that incorporation of hydrophilic glycolide units in L-lactide chains raises the alkaline and enzymatic hydrolyzabilities, whereas incorporation of hydrophobic epsilon-caprolactone units in L-lactide chains reduces the alkaline and enzymatic hydrolyzabilities. On the other hand, incorporation of D-lactide units with the same hydrophilicity of L-lactide units increases the alkaline hydrolyzability but decreases the enzymatic hydrolyzability. The alkaline hydrolyzability of the films of L-lactide copolymers with different kinds of comonomers and P(LLA-DLA) with different D-lactide unit contents can be closely related to their hydrophilicity. On the other hand, the enzymatic hydrolyzability of L-lactide copolymer films with different kinds of comonomers is mainly determined by hydrophilicity, while that of P(LLA-DLA) films is determined by the averaged L-lactyl and D-lactyl unit sequence lengths. The catalytic effect of proteinase K relative to that of alkali on the hydrolysis of P(LLA-DLA)(77/23) and P(LLA-GA)(81/19) films normalized by that of PLLA was lower than unity, whereas the normalized relative catalytic effect of proteinase K on the hydrolysis of P(LLA-CL)(82/18) film was higher than unity, meaning that despite low absolute alkaline and enzymatic hydrolyzability of the P(LLA-CL)(82/18) film, the catalytic effect of proteinase K may be maintained for this copolymer film, probably because of its blocky structure.

Calorimetry, Differential Scanning↗
PubMed2006

Poly(epsilon-caprolactone)/chitin and poly(epsilon-caprolactone)/chitosan blend films with compositional gradients: fabrication and their biodegradability.

Poly(epsilon-caprolactone) (PCL)/chitin and PCL/chitosan blend films with compositional gradients were successfully fabricated by a dissolution/diffusion method; that is, repeatedly pouring the PCL/chitin (or PCL/chitosan) blend solutions, with variable composition, onto polysaccharide layers. The compositional gradient structure in the resulting films was characterized by polarized optic microscopy, ATR-FT-IR and trans-FT-IR microscopic spectroscopy. Enzymatic degradability of the PCL/chitin and PCL/chitosan blend films with compositional gradients in the presence of lysozyme was compared with those of homogeneous films and two-layer films. It was found that the degradation rate of PCL/chitin blend films with a compositional gradient was far lower than that of the neat chitin film, whereas the degradation rate of PCL/chitosan blend films with a compositional gradient was close to that of the neat chitosan film. The suppression of the chitosan crystallization, which accelerates the enzymatic degradation, at the surface of PCL/chitosan films with a compositional gradient was much more severe than that for PCL/chitin films with a compositional gradient.

Biodegradation, Environmental↗
PubMed1998

The Effects of Caseinate Submicelles and Lecithin on the Thin Film Drainage and Behavior of Commercial Caseinate.

The drainage behaviour (stratification, thickness, and mobility) of thin foam films stabilized by commercial caseinate was studied in 10 mM phosphate buffer at pH 7.0. Thin films of commercial caseinate drained in a stepwise manner, with steps of similar thickness. The drainage was rapid, temperature sensitive, and chaotic, and the surface mobility of caseinate thin films also showed temperature sensitivity. The stepwise drainage is thought to be due to the layering of lecithin-caseinate submicelle complexes. Lecithin-stabilized thin films showed similar drainage behavior and temperature sensitivity. However, the films were approximately 66% thinner than caseinate films, and surface diffusion was very rapid. Removal of lipid from caseinate dramatically affects the thin film drainage properties and reduces temperature sensitivity. Reconstituted caseinate (i.e., extracted caseinate reconstituted with lipid), showed thin film properties similar to the commercial caseinate. Caseinate supplemented with lipid showed thin film drainage characteristics similar to caseinate, and surface mobility similar to lecithin. The presence of lecithin in caseinate thin films causes an increase in mobility, drainage, and stratification, along with a decrease in thin film thickness. This demonstrates that lecithin, possibly partially bound to the caseinate, is present at the interface disrupting protein-protein interactions. Copyright 1998 Academic Press.

Journal Article↗
PubMed1999

Direct Observation of Foam Film Rupture by Several Types of Antifoams Using a Scanning Laser Microscope.

It is well known that the stability of a pseudoemulsion film, a thin liquid film formed between an antifoam particle and air, can be important during defoaming action. We have compared the bursting behavior of a two-dimensional thin liquid film from an aqueous surfactant solution on a glass plate, in which six types of antifoam particles have been dispersed, using laser microscopic techniques. The used antifoams were a silicone oil, a mixed-type antifoam (mixture of silicone oil and hydrophobic solid particles), a hydrophobic silica, and a silicone-based solid antifoam (prepared by interfacial polymerization with oil and water). The antifoaming performance of these six types of antifoams, measured by the glass cylinder shaking test, was in the order: the mixed-type antifoam >== the silicone-based solid antifoam > the hydrophobic silica >== the silicone oil. Pseudoemulsion film rupture was observed at the film thickness less than 0.1 µm for both the silocone oil and the hydrophobic silica. In the case of particles with rough edges (the silicone-based antifoam), pseudoemulsion film on the top of the particles can be easily ruptured at a convex part of the solid surface. Furthermore, solid particles existing on the surface of an oil droplet in the mixed-type antifoams form marked projections and these projections give rise to distortion of the thinning film. As soon as the distortion of the thinning film took place on the top of the antifoam droplet, the pseudoemulsion film can be instantaneously ruptured. Referring to the antifoaming mechanisms for mixed-type antifoams, both steps from the pseudoemulsion film formation to the lens formation and from the counter pseudoemulsion film formation to the bridge formation would be very fast and cause a very high antifoaming efficiency. Copyright 1999 Academic Press.

Journal Article↗
PubMed1999

Hydrodynamic Instability of Liquid Films on Moving Fibers.

The stability of liquid films on moving fibers is studied with a focus on effects caused by film-solid adhesion interactions and hydrodynamic interactions between the film and the surrounding gas. We show that at high fiber velocities (large Reynolds numbers) the film-gas hydrodynamic interactions induce instability in films, which would, otherwise, be stabilized by the adhesion interactions at static conditions. Two types of unstable modes caused by hydrodynamic factors are found: the first corresponds to the Kelvin-Helmholtz waves induced by inertia effects; the second, induced by viscosity effects, is observed at smaller (yet still large) Reynolds numbers when the Kelvin-Helmholtz instability is suppressed. Linear stability analysis of the system of coupled hydrodynamic equations of film and gas flow is performed by the method of normal modes. We derive the general dispersion relation as an implicit equation with respect to the mode frequency. In the limit of vanishing fiber velocities, the obtained equation provides the dispersion equation for motionless fibers. The conditions of film stability and unstable modes are analyzed in terms of two dimensionless parameters, the adhesion factor, which quantifies the intensity of film-fiber interactions, and the Weber number, which quantifies the intensity of film-gas interactions. The Reynolds number determines the regions of validity of the inviscid and viscous regimes of film instability. The results are illustrated by estimates of the stability conditions for moving fibers in terms of the stability diagram, the critical film thickness, the fastest unstable mode, and the corresponding characteristic break-up time. Although the methods developed are applicable for any type of liquid-solid interaction, the estimates were made for the long-range van der Waals interactions. Practical applications include various technologies related to fabrication and chemical modifications of fibers and fiber products, e.g., spin finishing and lubrication. Copyright 1999 Academic Press.

Journal Article↗
PubMed1999

Packing Effect on Latex Film Dissolution: A UV-Visible Study.

Latex films with various thicknesses are formed from pyrene (P) labeled poly (methyl methacrylate) (PMMA) latex particles sterically stabilized by poly isobutylene (PIB). Annealings of latex films were performed above T(g) at elevated temperatures up to 270 degrees C for 30 min time intervals. The UV-Visible (UVV) technique was used for monitoring latex film formation and dissolution. It was observed that thicker films formed more transparent films than thinner films. Absorption of solvent molecules (chloroform) into the annealed latex film was followed by diffusion of PMMA chains into a solvent reservoir. Diffusion of pyrene-labeled PMMA chains was monitored in real time by the absorbance change of pyrene in the polymer-solvent mixture. A diffusion model with a moving boundary was employed to quantify real-time UVV data. Diffusion coefficients of PMMA chains were measured and found to be between 2.6 x 10(-9) and 9.7 x 10(-13) cm(2) s(-1) for the latex films in various thicknesses. It is observed that thicker and more transparent films dissolved much faster than the thinner and turbid films; i.e., highly packed films dissolve more easily. Copyright 1999 Academic Press.

Journal Article↗
PubMed2003

Productivity and cost assessment of computed radiography, digital radiography, and screen-film for outpatient chest examinations.

An objective assessment and comparison of computed radiography (CR) versus digital radiography (DR) and screen-film for performing upright chest examinations on outpatients is presented in terms of workflow, productivity, speed of service, and potential cost justification. Perceived ease of use and workflow of each device is collected via a technologist opinion survey. Productivity is measured as the rate of patient throughput from normalized timing studies. The overall speed of service is calculated from the time of examination ordering as stamped in the radiology information system (RIS), to the time of image availability on the picture archiving and communication system (PACS), to the time of interpretation rendered (from the RIS). A cost comparison is discussed in terms of potential productivity gains and device expenditures. Comparative results of a screen-film (analog) dedicated chest unit versus a CR reader and a DR dedicated chest unit show a higher patient throughput for the digital systems. A mean of 8.2 patients were moved through the analog chest room per hour, versus 9.2 patients per hour using the CR system and 10.7 patients per hour with the DR system. This represents a 12% increase in patient throughput for CR over screen-film; a 30% increase in patient throughput for DR over screen-film, which is statistically significant; and a 16% increase in patient throughput for DR over CR, which is not statistically significant. Measured time to image availability for interpretation is much faster for both CR and DR versus screen-film, with the mean minutes to image availability calculated as 29.2 +/- 14.3 min for screen-film, 6.7 +/- 1.5 min for CR, and 5.7 +/- 2.5 min for DR. This represents an improved time to image availability of 77% for CR over screen-film, 80% for DR over screen-film, and 15% for DR over CR. These results are statistically significant (P <.0001) for both CR over screen-film and DR over screen-film but not statistically significant for DR over CR. A comparison of the digital technology costs illustrates that the high cost of DR may not be justifiable unless a facility has a steady high patient volume to run the device at or near 100% productivity. Both CR and DR can improve workflow and productivity over analog screen-film in a PACS for delivery of projection radiography services in an outpatient environment. Cost justification for DR over CR appears to be tied predominantly to high patient volume and continuous rather than sporadic use patterns.

Ambulatory Care Facilities↗
PubMed1990

Cellular invasion and breakdown of three different collagen films in the lumbar muscle of the rat.

Collagen films were prepared by three different methods involving acid homogenization at pH 3.0 of a collagen suspension for 1.5 min (film A) and 15 min (film B) and alkaline homogenization at pH 10 for 15 min (film C), after which the resulting slurries were degassed and dried over sterile air. Subsequent examination by scanning electron microscope (SEM) revealed that all samples showed a distinctly layered structure which was much finer in the acid films. Implantation into the lumbar muscle of rats followed by histology and SEM studies revealed that film B was completely resorbed at 14 d whereas remnants of film A could still be seen at this period. The slowest rate of resorption was observed with film C, traces of which could still be found at 70 d. Invading inflammatory cells moved into the collagen films between the layers from the edges only causing the whole structure to 'ribbon out'. The surfaces of all three films appeared to be impenetrable to cells. Incubation of the three films with bacterial collagenase revealed similar relative rates of degradation to those observed in vivo.

Absorption↗
PubMed2004

Study on the enhancement of catalytic activity for hemoglobin by quinhydrone in poly(o-aminophenol) film.

Hemoglobin (Hb) and quinhydrone (QHQ) were incorporated in poly(o-aminophenol) [o-AP, POAP] film by electropolymerization of o-aminophenol in a weak acid solution containing Hb and QHQ. The nonconducting polymer film was found to be nearly rigid by piezoelectric quartz crystal (PQC) impedance. Therefore, the thickness of the Hb-QHQ-POAP film was estimated as about 104 +/- 10 nm by quartz crystal microbalance (QCM). The QHQ mediation effects on the biomacromolecule Hb entrapped in the POAP film were investigated by using cyclic voltammetry, amperometric technique and kinetic study. Cyclic voltammograms showed that the redox peaks in the Hb-QHQ-POAP film are much more reversible than those in the Hb-POAP film. The response current of the Hb-QHQ-POAP film to H(2)O(2) was almost twice than that of the Hb-POAP film. The Michaelis-Menten constant and the activation energy of Hb in the Hb-QHQ-POAP film are 7.47 mM and 13.91 kJ/mol, respectively, both are smaller than that in the Hb-POAP film. These results showed that the immobilized Hb in POAP film exhibited higher catalytic activity to H(2)O(2) due to the mediation of QHQ.

Aminophenols↗
PubMed2006

Layer-by-layer films of hemoglobin or myoglobin assembled with zeolite particles: electrochemistry and electrocatalysis.

Positively charged hemoglobin (Hb) or myoglobin (Mb) at pH 5.0 in solutions and negatively charged zeolite particles in dispersions were alternately adsorbed onto solid surfaces forming [zeolite/protein](n) layer-by-layer films, which was confirmed by quartz crystal microbalance (QCM) and cyclic voltammetry (CV). The protein films assembled on pyrolytic graphite (PG) electrodes exhibited a pair of well-defined, nearly reversible CV peaks at about -0.35 V vs. SCE at pH 7.0, characteristic of the heme Fe(III)/Fe(II) redox couples. Hydrogen peroxide (H(2)O(2)) and nitrite (NO(2)(-)) in solution were catalytically reduced at [zeolite/protein](7) film modified electrodes, and could be quantitatively determined by CV and amperometry. The shape and position of infrared amide I and II bands of Hb or Mb in [zeolite/protein](7) films suggest that the proteins retain their near-native structure in the films. The penetration experiments of Fe(CN)(6)(3-) as the electroactive probe into these films and scanning electron microscopy (SEM) results indicate that the films possess a great amount of pores or channels. The porous structure of ]zeolite/protein](n) films is beneficial to counterion transport, which is crucial for protein electrochemistry in films controlled by the charge-hopping mechanism, and is also helpful for the diffusion of catalysis substrates into the films. The proteins with negatively charged net surface charges at pH 9.0 were also successfully assembled with like-charged zeolite particles into layer-by-layer films, although the adsorption amount was less than that assembled at pH 5.0. The possible reasons for this were discussed, and the driving forces were explored.

Adsorption↗
PubMed2005

Core--shell nanocluster films of hemoglobin and clay nanoparticle: direct electrochemistry and electrocatalysis.

A novel core-shell protein nanocluster film, designated as clay-(Hb/PSS)(n), was fabricated on pyrolytic graphite (PG) electrodes. Positively charged hemoglobin (Hb) at pH 5.5 and negatively charged poly(styrenesulfonate) (PSS) were first assembled layer by layer on surface of clay nanoparticles from their solutions mainly by electrostatic attraction, forming a core-shell nanocluster structure in which clay nanoparticles were the "cores" and (Hb/PSS)(n) multilayers were the "shells". The aqueous dispersion of clay-(Hb/PSS)(n) nanoclusters was then cast on surface of PG electrodes, forming clay-(Hb/PSS)(n) nanocluster films after evaporation of solvent. Hb in clay-(Hb/PSS)(n) films exhibited a pair of well-defined and reversible cyclic voltammetric (CV) peaks at about -0.36 V vs. SCE in pH 7.0 buffers, characteristic of Hb heme Fe(III)/Fe(II) redox couples. Compared with other Hb-containing clay films, clay-(Hb/PSS)(n) films displayed smaller CV peak separation (DeltaE(p)), indicating the better electrochemical reversibility of Hb in these nanocluster films. The partially ordered structure of the films was characterized by X-ray diffraction (XRD) experiments. UV-VIS and reflection absorption infrared (RAIR) spectroscopy suggests that Hb retains its near-native structure in clay-(Hb/PSS)(n) films. Oxygen, hydrogen peroxide, and nitrite were catalytically reduced at clay-(Hb/PSS)(n) film electrodes, showing the potential applicability of the films as the new type of biosensors or bioreactors based on protein direct electrochemistry. The electrochemical and electrocatalytic activity of the films could be tailored by controlling the number of bilayers of the (Hb/PSS)(n) shells on the surface of clay nanoparticle cores.

Aluminum Silicates↗
PubMed2006

Surface functionalized titanium thin films: zeta-potential, protein adsorption and cell proliferation.

The relationship between electric charge at a material surface and protein adsorption is essential to understand the mechanism of biological integration of materials with tissues. This study investigated the influence of titanium thin films' surface chemistry and surface electric charge (zeta-potential) properties on protein adsorption and cell proliferation. Titanium thin films were surface functionalized with different functional end groups, such as -CH=CH2, -NH2 and -COOH groups in order to produce surfaces with a variety of electric charge properties. The chemical compositions, electric charges and wettability were investigated by using X-ray photoelectron spectroscopy (XPS), zeta-potential measurements and water contact angle measurements, respectively. XPS revealed the surface functionalization of titanium films with -CH=CH2, -NH2, and -COOH groups, which were converted from -CH=CH2 groups. Ti-COOH samples showed the lowest water contact angles and zeta-potential compared to all other samples investigated in this study. NH2-terminated titanium films displayed intermediate contact angles of 70.3+/-2.5 degrees . Fibrinogen adsorption on titanium films and surface functionalized titanium films were investigated in this study. Ti-COOH samples displayed a lower protein adsorption than all other groups, such as NH2-, -CH=CH2-terminated titanium thin films. A tendency that the lower zeta-potential of the samples, the lower the protein adsorption at their surfaces was observed. In vitro cell proliferation tests were also performed on the different surface functionalized titanium films. NH2-terminated titanium films displayed good cell proliferation and cell viability tendency. However, a lower cell proliferation on COOH-terminated titanium films was observed compared with NH2-terminated titanium films. This effect was attributed to the difference in protein adsorption of these samples.

Adsorption↗
PubMed2005

Film drainage and interfacial instabilities in polymeric systems with diffuse interfaces.

We report an experimental investigation on the effect of mutual diffusion in polymeric systems on film drainage between two captive drops. The main objective is to study the influence of diffuse interfaces on film drainage. This is done by using material combinations with different interfacial properties and interferometric visualization of the film between two interacting drops. For highly diffusive systems film drainage is observed to be, in contrast to immiscible systems, non-axisymmetric and unstable immediately after the film formation (at a few micrometers film thickness). Depending on whether the total thickness of the diffusion layers in the film is smaller or larger than the thickness of the film, Marangoni convection is found to enhance or delay film drainage. Enhanced film drainage is determined to be in order of 100 times faster than predicted by the current models, while delayed film drainage is observed after a drainage period where experimental and predicted results (assuming, a partially mobile interface) are in close agreement.

Journal Article↗
PubMed2006

Aqueous foam films stabilized by sodium naphthenates.

Stratification of a foam liquid film drawn from aqueous solutions of sodium naphthenate at relatively high concentration is likely due to a lamellar liquid crystal-like structure within the film. Film stratification, resulting in stepwise thinning, has been observed in foam films formed from systems containing either moderate to high concentrations of surfactant or in films formed from solutions containing solid particles. At moderate surfactant concentrations, film stratification is likely due to layers of ordered spherical micelles as postulated in Wasan and Nikolov's model of film stratification. At high surfactant concentrations, stepwise thinning of the films and occurrence of domains of uniform color within the film suggest a lamellar liquid crystal-like structure within the film, potentially up to hundred or more oriented layers. The LLC-like structure inside the film can occur at concentrations below the lower limit of the LLC existence as a bulk phase.

Journal Article↗
PubMed1997

A phase I comparative study of three contraceptive vaginal films containing nonoxynol-9. Postcoital testing and colposcopy.

The objectives of this study were 1) to assess the ability of a new contraceptive vaginal film containing two doses of nonoxynol-9 (N-9) to prevent the penetration of sperm into midcycle cervical mucus, and 2) to determine the effect of the film on the vaginal epithelium. The novel formulation was compared with VCF (a currently marketed film also containing N-9). Ten women underwent two baseline cycles of postcoital testing in which no film was used, followed by three test cycles in which Allendale-N9 film, a new film containing either 100 or 130 mg N-9, or VCF containing 70mg N-9 was used. The sequence of testing cycles was randomized. In each cycle, condoms were used prior to midcycle, then a midcycle cervical mucus specimen was examined to ensure midcycle characteristics and the absence of sperm. Each woman then had intercourse using either no film (baseline cycles) or a test film (test cycles) and returned 2-3 h afterwards. Cervical mucus was again assessed for adequacy and the presence of sperm. Each woman also underwent colposcopy using a protocol developed by the World Health Organization. The average number of progressively motile sperm seen per high power field were as follows: average of the two baseline cycles, 19.3; test cycle with Allendale-N9 film containing 100 mg N-9, 0.6; test cycle with Allendale-N9 film containing 130 mg N-9, 0.9; and test cycle with VCF, 0.5. There was no significant difference between baseline cycles or between test cycles in the number of progressively motile sperm per high power field (HPF) seen (p = 0.31 and p > or = 0.50, respectively). The average number of motile sperm seen in each test cycle did, however, differ significantly from the number in either baseline cycle (p < 0.02). The majority of colposcopic examinations were normal. In one baseline cycle and eight test cycles, colposcopy showed superficial de-epithelialization without underlying inflammation. There was no apparent dose response and in all cases the volunteers were asymptomatic. A vaginal contraceptive containing either 100 or 130 mg N-9 in a new film base appears to be safe and comparable to VCF in preventing sperm from entering midcycle cervical mucus.

Administration, Intravaginal↗