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Experimental Therapeutics, Preclinical Pharmacology |
1 Department of Pathology and Laboratory Medicine and the 2 College of Pharmacy, the University of Cincinnati, Cincinnati, Ohio
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ABSTRACT |
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 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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The effectiveness of fibrinogen-coated, docetaxel-loaded oil droplets against a solid tumor like the melanoma prompted us to consider whether the droplets might also be effective against less consolidated tumors (e.g., ascites tumors) that are especially prone to fibrin(ogen) deposition (7) . An example is the TA3/St ascites tumor, which derived from a spontaneous mammary carcinoma in a mouse of the A/HeHa strain (8 , 9) . Because its microenvironment is so fibrin(ogen)-rich, we felt the TA3/St tumor might be ideally suited to treatment with fibrinogen-coated olive oil droplets loaded with docetaxel, an agent particularly effective against mammary carcinomas (10 , 11) .
In this report, we describe studies in which the TA3/St mammary tumor grown in ascites form was used to compare the anticancer activity of docetaxel delivered in fibrinogen-coated olive oil droplets to that of docetaxel administered as its standard formulation, Taxotere. Because the therapeutic benefit conferred by the fibrinogen-coated oil droplets was substantial, additional studies were done to elucidate the role of thrombin activity/fibrin formation in the operation of the droplets, and to determine whether the droplets elicit antifibrinogen antibodies that are of obvious clinical consequence.
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Mice.
Eight- to 10-week-old female A/Jax mice weighing between 17 and 20 g were from The Jackson Laboratory (Bar Harbor, ME). Before use, mice were acclimated to the local environment for a period of 1 week. The animal protocol was reviewed and approved by the Institutional Animal Care and Use Committee of the University of Cincinnati.
Tumor Cells.
TA3/St ascites tumor cells were from Drs. Janice Nagy and Harold Dvorak (Boston, MA). Tumor cells were propagated as stock cultures within the abdominal cavities of A/Jax mice. Tumor cells intended for administration to test animals were collected from the abdominal cavities of three mice that had carried tumor cells for 5 days. Tumor cells from the three animals were pooled, and then washed once using 20 mL of normal saline (NS) and centrifugation at 1,500 x g for 3 minutes. Before inoculating them into naive mice, tumor cells were dispersed in NS to a final concentration of 1 x 106 cells · mL–1. The volume of a tumor cell inoculum was always 1 mL.
Preparation of Emulsions.
When included in an olive oil preparation, docetaxel was first dissolved in the oil phase to a final concentration of 1 mg · mL–1 with an ultrasonic water bath and intermittent sonication over the course of 1 hour. As determined by using high performance liquid chromatography, such sonication does not result in any discernible deterioration of docetaxel (6)
.
Both drug-free and drug-loaded olive oil were emulsified with the method of high pressure extrusion (3
, 6)
. Two mL of drug-free or drug-loaded olive oil and 3 mL of NS containing F68 at a concentration of 1 mg · mL–1 were added to a clean, 12 x 75-mm glass tube. The oil/water mixture was gently agitated and was then extruded 5 times under high pressure, 103.5 MPa, through the aperture of a homogenizer (EmulsiFlex-20,000-B3; Avestin, Ottawa, Canada). To the resulting oil-in-water emulsion was immediately added either 2 mL of NS or 2 mL of NS containing murine fibrinogen, human fibrinogen or BSA. Because murine fibrinogen from commercial source is exceedingly expensive, we reduced the concentration of all proteins used to coat droplets from 4 mg · mL–1 (6)
to 2 mg · mL–1. After sonicating the emulsion for 10 to 15 seconds with an ultrasonic water bath, centrifugation at 1,500 x g for 15 minutes was used to float the oil droplets. The resulting infranatant was removed, and an ultrasonic water bath was used to disperse the residual cream layer in 3 mL of NS. The volume of emulsion used for an injection was 1 mL, of which 40% was olive oil. Oil droplets prepared in this fashion are polydisperse in size, ranging in diameter from 
1 to 100 µm, with a mean diameter of 12 µm (6)
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Unless specified otherwise, NS as diluent was used to prepare Taxotere for injection to a final concentration of 0.40 mg · mL–1.
Tumor Model and Treatments and Toxicity Assessment.
To begin an experiment, mice received an injection intraperitoneally with tumor cells. Three days later, a single inoculum of test or control material was then administered intraperitoneally to the animals. Whether in oil droplets or as Taxotere, the amount of docetaxel administered per test inoculum was always 0.40 mg (i.e., 20 mg/kg animal body mass). Regardless of material/vehicle, the total volume per injection was always 1 mL.
For some experiments, Refludan was administered to tumor-bearing mice. The first dose was administered intraperitoneally 2 hours before treating animals with test or control materials. Thereafter, tumor-bearing mice received a similar bolus at 24 hour intervals on all subsequent days. Before injection, the Refludan was diluted with NS. The amount of Refludan administered each time was 40 µg in 0.2 mL.
To assess toxicity, a separate experiment was done in which healthy, tumor-free mice of known weights were treated in groups of five, each with a single intraperitoneal injection of one of several preparations. Using a top-loading balance, we measured the weights of the animals every day for 15 days. Statistical significances of differences between mean weights of mice from the various treatment groups were determined by using Student’s t test. We took as significant P 
0.05.
Analysis of Antitumor Efficacy Data.
The number of mice surviving in an experimental group was monitored as a function of time after tumor cell inoculation. Results of survival studies were plotted as the percentage of animals remaining alive in a group versus day after tumor cell inoculation. For purposes of inter-group comparisons, the percentage of increase in life span (%ILS) because of a treatment was defined as [(median days of survival of treated group – median days of survival of NS-treated group)/median days of survival of NS-treated group] x 100%. Statistical significances of differences between mean survival times of various treatment groups were determined by using Student’s t test. Again, we took as significant P 0.05.
Abdominal Cavity Lavage and Recovery and Evaluation of Ascites/Lavage Fluid.
Mice that had been treated variously were euthanized and, immediately thereafter, each was given an intraperitoneal inoculum of 2 mL NS. Three-milliliter plastic syringes equipped with 18 gauge needles were then used to collect as much of the lavage fluids and their accompanying materials as possible from the abdominal cavities of the animals. Lavage fluid recovered from an animal was used in various ways. Sometimes it was immediately spread onto glass microscope slides and either covered with a glass coverslip for viewing using phase-contrast microscopy or stained with oil red O (13)
and covered with a glass coverslip for viewing. For one set of experiments, centrifugation at 1,500 x g for 10 minutes was used to clear lavage fluids of cells, and a turbidimetric method (14)
was used to assess the thrombin activities in 20–50 µL aliquots of the resulting cell-free fluids. In brief, the turbidimetric method involves adding a test sample to a stirred dispersion of fibrinogen-coated, microscopic latex beads. Such beads agglutinate in the presence of thrombin, a consequence of interbead fibrin formation. A platelet aggregometer or other photometric device can be used to monitor agglutination. The rate of change of light-scattering of the stirred bead dispersion is proportional to the thrombin activity in the sample. Thrombin-inducible agglutination of fibrinogen-coated beads is inhibited in stoichiometric fashion by hirudin, a thrombin specific inhibitor (14)
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Monitoring the Association of Docetaxel with Tumor Cells.
[3H]docetaxel was added to both oil droplets and Taxotere. When included in oil droplets, [3H]docetaxel was added along with unlabeled docetaxel to the oil just before emulsification of that phase. When included in Taxotere, [3H]docetaxel was added to the ethanolic polysorbate 80 of the commercial preparation just before dilution of that material with NS.
Three days after administering tumor cells to mice, tumor-bearing animals were each given an intraperitoneal injection of the radioactively spiked version of either Taxotere or docetaxel-loaded oil droplets. Some oil droplet-treated mice were also treated with Refludan as described above. Twenty-four or 48 hours later, all of the animals of a group were sacrificed, their abdominal cavities were lavaged, and the lavage fluids and accompanying materials were collected as described above. After determining the number of cells in a lavage sample, centrifugation at 1,500 x g for 2 minutes was used to sediment the cells in the sample. The radioactivity associated with the cells was then measured after diluting them with liquid scintillation medium. Results were recorded as nanograms of docetaxel per 1,000 recovered tumor cells.
Immunodetection of Proteins.
Immunoblotting was used to detect thrombin in fluids recovered from the abdominal cavities of tumor-bearing mice. Mice that had received injection with tumor cells were euthanized after various lengths of time. Immediately after euthanizing an animal, its abdominal cavity was inflated with 2 mL of NS. The lavage and accompanying ascites fluid were then collected by using a 3-mL plastic syringe equipped with an 18 gauge needle. Centrifugation at 1,500 x g for 15 minutes was used to sediment tumor cells, and the cell-free fluid was aspirated and saved. Ten microliters of the aspirate were blotted alongside control materials onto a polyvinylidene difluoride membrane (Immobilon-P, Millipore, Bedford, MA). After drying a membrane at room temperature for 1 hour, it was immersed for 30 minutes in 60 mL of buffer containing 0.02 mol/L Tris-HCl (pH 7.5), 0.15 mol/L NaCl, 0.05% (v/v) Tween 20, and 40 mg · mL–1 of BSA. Subsequently, membranes were rinsed with water and treated, first with rabbit antithrombin IgG as primary (1°) antibody and then with AP-conjugated, goat antirabbit IgG as secondary (2°) antibody. Substrates for AP activity were from Promega.
Immunoblotting was also used to detect fibrinogen both on washed tumor cells and on washed oil droplets. Mice that had received injection intraperitoneally 3 days earlier with tumor cells were treated, each with 1 mL of a test emulsion. One hour later, the mice were euthanized, after which each was given an intraperitoneal injection of 2 mL of NS. Three-milliliter plastic syringes equipped with 18 gauge needles were used to collect lavage fluids from the abdominal cavities of the mice. Centrifugation at 1,500 x g for 15 minutes was used to sediment and float tumor cells and oil droplets in fluids, respectively. Tumor cell and oil droplet fractions were isolated, and a stirred flow cell (10 mL, Amicon, Danvers, MA) equipped with a polycarbonate filter (Sigma) with pores of diameter 1.2 µm was used to wash the cells or oil droplets 8 times. The washing medium was NS containing 10 mg · mL–1 of BSA. One milliliter of NS was used to rinse washed oil droplets from a filter. Ten microliters of the resulting dispersion of oil droplets were blotted alongside positive and negative control materials onto a polyvinylidene difluoride membrane. NS was used to rinse washed tumor cells from a filter, and then cells were resuspended in that medium to a final concentration of 1 x 106 cells · mL–1. Ten microliters of tumor cell suspension was blotted alongside control materials onto a polyvinylidene difluoride membrane. After drying a membrane at room temperature for 1 hour, it was immersed for 30 minutes in 60 mL of buffer containing 0.02 mol/L Tris-HCl (pH 7.5), 0.15 mol/L NaCl, 0.05% (v/v) Tween 20, and 40 mg · mL–1 of BSA. Subsequently, membranes were rinsed with water and treated first with rabbit antifibrinogen IgG as 1° antibody and then with AP-conjugated, goat antirabbit IgG as 2° antibody. Substrates for AP activity were from Promega.
Elicitation and Assessment of Antifibrinogen Antibodies.
Mice in groups of 3 to 6 received injection intraperitoneally at time 0 and after 7, 14, and 21 days with one of several preparations. The preparations included (a) NS, 1 mL; (b) emulsion containing docetaxel-free, fibrinogen-free oil droplets, 1 mL; (c) emulsion containing docetaxel-free oil droplets coated with murine fibrinogen, 1 mL; (d) emulsion containing docetaxel-free oil droplets coated with human fibrinogen, 1 mL; (e) Freund’s incomplete adjuvant, 0.4 mL, containing 1 mg of murine fibrinogen in NS; and (f) Freund’s incomplete adjuvant, 0.4 mL, containing 1 mg of human fibrinogen in NS. After 38 days, heparinized Natelson capillary tubes were used to collect blood samples from the retro-orbital plexuses of treated mice. Blood was also collected in similar fashion from age-matched untreated mice. After centrifugation of the blood samples at 1,500 x g for 12 minutes, ELISA was used to assess the plasma from each for antifibrinogen antibodies.
For the ELISA, 96-well flat-bottomed microtiter plates (PRO-BIND, Becton Dickinson, Franklin Lakes, NJ) were prepared and used as follows. Into each well of a plate was added 150 µL of 0.05 mol/L carbonate buffer (pH 9.60), containing 100 µg · mL–1 of fibrinogen. Depending on the experiment, either human or murine fibrinogen was used. Before using the murine fibrinogen, we removed the IgG that contaminated the protein by using a 1 mL Protein G Sepharose column (HiTrap Protein G HP, Amersham Biosciences) according to the column’s manufacturer. The solution containing the appropriate species-specific fibrinogen was incubated in the wells of a plate for 2 hours at room temperature. After that time, the fibrinogen-containing solution was forcibly ejected from the wells. "Blocking" medium, 250 µL, containing 0.01 mol/L phosphate buffer (pH 7.40), 0.15 mol/L NaCl, 0.1% (v/v) Tween 20, 10 mg · mL–1 of casein and 20 mg · mL–1 of BSA was next added to each well of the plate, which was then left undisturbed for 60 minutes. After forcibly ejecting the blocking medium and rinsing the wells four times with phosphate-buffered saline containing 0.1% (v/v) Tween 20, the plate was ready for the addition of plasma samples. Plasma samples to be assessed for antifibrinogen antibody content were prediluted 1:5, v/v, with 0.1 mol/L HEPES buffer (pH 7.40) containing 0.10 mol/L NaCl, 10 mg · mL–1 BSA, and 0.1% (v/v) Tween 20. A 250 µL aliquot of such a dilution was added to the first well of a row of wells on a fibrinogen-coated plate. To each of the remaining wells of a row was added 125 µL of the HEPES-buffered dilutent. Two-fold serial dilution of the content of the first well was then done, out to a maximum of 24 wells. The dilutions of plasma were incubated in the wells for 1 hour at room temperature, after which the dilutions were forcibly ejected, and the wells were rinsed 4 times with a buffer containing 0.1% (v/v) Tween 20. One hundred and fifty microliters of a 1:2,500 dilution of horse radish peroxidase-conjugated goat antimouse IgG was next added to each well and incubated there at room temperature for 1 hour. After that time, the IgG-containing solution was ejected from the wells, and the plates were rinsed 4 times with buffer containing 0.1% (v/v) Tween 20 before adding o-phenylenediamine (Sigma) as colorimetric substrate for horse radish peroxidase. The end point titer of the antifibrinogen antibodies was determined from visual inspection of the intensity of color in the wells after 20 minutes.
Assessment of the Coagulability of Citrated Plasma Samples.
Blood samples from the retro-orbital plexuses of mice were collected by using plain Caraway blood collecting tubes that had each been preloaded with 5 µL of 0.105 mol/L (i.e., 3.2%, w/v) buffered citrate solution. The volume of blood collected within a tube was 270 µL. Within 3 seconds of having collected a blood sample, it was discharged into a 0.5 mL conical polypropylene tube containing 30 µL of 0.105 mol/L buffered citrate. Centrifugation at 15,000 x g for 5 minutes was used to separate citrated plasma from blood cells. The activated partial thromboplastin times (aPTTs) of the citrated plasma samples were determined by technologists of the Investigative Hemostasis Laboratory of the University of Cincinnati Medical Center who used for those determinations actin FSL (Dade Behring, Deerfield, IL) and an automated coagulation analyzer (BCS, Dade Behring).
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RESULTS |
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After first demonstrating that the survival benefit conferred to TA3/St tumor-bearing mice by docetaxel-loaded oil droplets coated with either murine or human fibrinogen was the same (P = 0.40, data not shown), we then compared that survival benefit to those conferred by other preparations, including NS, docetaxel-free oil droplets coated with either BSA or murine fibrinogen, Taxotere, docetaxel-loaded oil droplets coated with BSA, or docetaxel-loaded oil droplets that had not been coated with any protein. As shown in Fig. 1
, the survival plots related to NS and docetaxel-free droplets of olive oil were virtually superimposable, the differences in mean survival times not being statistically significant (P 
0.80). For mice in those groups, the median time to death (MTTD) was 9.5 days. Taxotere-treated mice lived significantly longer than vehicle-treated mice (P = 0.0002), their MTTD being 14.5 days (%ILS = 53). Mice treated with BSA-coated droplets of docetaxel-loaded olive oil lived significantly longer (P = 0.035, MTTD = 20 days, %ILS = 111) than Taxotere-treated mice, but not as long as mice treated with either uncoated droplets of docetaxel-loaded olive oil (P = 0.007, MTTD = 25 days, %ILS = 163) or docetaxel-loaded oil droplets coated with murine fibrinogen (P = 0.0001, MTTD = 29.5 days, %ILS = 211). Although the MTTD’s of the last 2 groups were different and their survival profiles overlapped only slightly, the mean times to death of animals in the 2 groups (i.e., 24.8 ± 2.8 days for mice treated with uncoated droplets and 28.4 ± 4.7 days for mice treated with fibrinogen-coated droplets) were not significantly different, P = 0.082. This last finding was not unexpected (6)
, and is addressed below. We conclude that droplets of olive oil, particularly ones precoated with fibrinogen, are better vehicles for the intraperitoneal delivery of docetaxel to the ascites form of the TA3/St mammary tumor than ethanolic polysorbate 80, the medium within which docetaxel is formulated commercially.
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As a preliminary assessment of toxicity, we monitored for 15 days the weights of healthy, tumor-free mice treated with either NS, Taxotere, or fibrinogen-coated droplets of docetaxel-loaded olive oil. At each daily weighing, there were no statistically significant differences between the average weights of animals of any of the treatment groups. With respect solely to recipient weight, we conclude that a single intraperitoneal injection of fibrinogen-coated droplets of docetaxel-loaded olive oil is no more harmful to mice in the short term than is a single intraperitoneal injection of NS.
Thrombin Activity in Ascites Fluid from Tumor-Bearing Mice.
Fibrinogen-coated droplets of olive oil were developed by us as vehicles with which to deliver oil-soluble drugs to sites of fibrin formation. We expected thrombin activity existing at such sites would facilitate incorporation there of the droplets into nascent fibrin clots. Because fibrin accumulates within the abdominal cavities of A/Jax mice bearing the ascites form of the TA3/St mammary tumor (7)
, we anticipated thrombin would be present in ascites fluids of tumor-bearing animals. Indeed, thrombin was present both antigenically (data not shown) and functionally, Fig. 2
, in cell-free ascites/lavage fluids recovered from tumor-bearing mice. On average (n = 3), the thrombin activity recovered from a tumor-bearing mouse after 3 days was 0.019 ± 0.009 units/mL of recovered fluid. After 5 days, the thrombin activity had increased significantly (P 0.05) to 0.053 ± 0.015 units/mL of recovered fluid. No thrombin activity was detected in lavage fluids recovered from healthy, tumor-free mice (n = 3).
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and 3
. Because the half-life of hirudin in vivo is short, t1/2 = 1.3 hours (15)
and because we found the thrombin activity in the abdominal cavities of tumor bearing-mice to be high, we administered a rather large dose of hirudin (Refludan), 40 µg, each day to each test animal. On the basis of drug mass per unit recipient mass, that amount of hirudin corresponds to approximately 4 times the usual loading dose of the drug when it is used in humans (15)
. As shown in the figure, whereas the daily administration of hirudin by itself had no statistically significant effect (P = 0.25) on the survival of tumor-bearing mice, it did reduce the survival benefit of mice treated with any of the docetaxel-loaded oil droplets to that of mice treated with Taxotere (P 0.80). Taken together, these results suggest fibrin formation at the surface of the oil droplets contributes to the survival benefit conferred by docetaxel-loaded droplets of olive oil, whether the droplets are precoated with fibrinogen or not.
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0.001). Furthermore, and consistent with the results of the survival studies, if hirudin is coadministered with fibrinogen-coated droplets of docetaxel-loaded olive oil, the association after 2 days of the drug with tumor cells is reduced significantly (P 0.02) from that observed in the absence of the thrombin inhibitor.
Association of Oil Droplets with Tumor Cells In vivo.
If fibrin does mediate the binding of drug-loaded oil droplets to tumor cells, then one might expect to see oil droplets adhered to tumor cells recovered from oil droplet-treated mice. Furthermore, hirudin should prevent such adherence. As shown in Fig. 4
, rosettes consisting of oil droplets and tumor cells were abundant in ascites removed from tumor-bearing mice shortly after having administered to the animals either fibrinogen-coated droplets or uncoated droplets. Coadministration of hirudin with either of those droplets prevented rosette formation. Although the association of BSA-coated droplets with tumor cells was much less obvious than that seen when using either fibrinogen-coated droplets or uncoated droplets, such association was still present and sensitive to hirudin. We conclude that fibrin does indeed mediate the binding of oil droplets to tumor cells.
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). Using an immunoblotting technique, we found, as expected, that both uncoated droplets and BSA-coated droplets acquire in vivo a layer of endogenous fibrin(ogen), Fig. 5A
. Importantly, not only the droplets, but also the ascites tumor cells are coated with fibrin(ogen), Fig. 5B
. Because fibrin molecules on juxtaposed microparticles can interact to cause the mutual adhesion of the particles (2
, 14)
, our results suggest oil droplets are tethered to tumor cells by fibrin polymers that are themselves anchored to the two surfaces.
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. Although significantly higher titers of antifibrinogen antibodies were achieved when human fibrinogen was used as coating than when murine fibrinogen was used as coating (P 0.001), the levels of antifibrinogen antibodies in both cases were appreciable. Perhaps not surprisingly, two of five mice treated with uncoated oil droplets had demonstrable, albeit low, levels of antibodies directed against murine fibrinogen. These findings prompted investigation of the biological consequences of antifibrinogen antibodies in mice treated with fibrinogen-coated oil droplets.
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, the presence of even very high levels of droplet-induced antifibrinogen antibodies did not prolong the survival of tumor-bearing animals beyond that yielded by Taxotere alone (P = 0.26). Such a result suggests antifibrinogen antibodies play no role in the therapeutic efficacy of docetaxel when the drug is delivered within fibrinogen-coated droplets of olive oil.
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DISCUSSION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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If left untreated, mice bearing the ascites form of the TA3/St mammary tumor all die by 10 days. Whereas Taxotere prolongs the median survival of tumor-bearing mice by 53%, docetaxel delivered in microscopic droplets of olive oil prolongs median survival by as much as 211% (i.e., a 4-fold improvement over Taxotere). Several experiments indicate droplet-bound fibrinogen and its conversion to fibrin are responsible for the efficacy of docetaxel-loaded oil droplets. Briefly, maximal survival benefit is achieved when droplets are precoated with fibrinogen, and a measure that inhibits thrombin activity (i.e., a measure that inhibits fibrinogen-to-fibrin conversion) reduces the survival benefit of docetaxel-loaded oil droplets to that of an equivalent dose of docetaxel administered as Taxotere. It is not surprising that even uncoated or BSA-coated droplets confer a hirudin-sensitive benefit to survival that is greater than that conferred by Taxotere, because endogenous fibrinogen coats those droplets, rendering them equivalent operationally to droplets precoated with fibrinogen. The survival benefits conferred by uncoated droplets and BSA-coated droplets are somewhat less than that conferred by droplets precoated with fibrinogen because in the former cases extraneous proteins limit the packing density of endogenous fibrinogen. We conclude that microscopic droplets of olive oil, particularly ones precoated with fibrinogen, are a more effective means by which to deliver docetaxel to the ascites form of the TA3/St mammary tumor than is Taxotere. It seems the conversion of droplet-bound fibrinogen to fibrin by thrombin acting locally facilitates the specific adherence of drug-loaded droplets to tumor cells and, perhaps, the general retention of droplets within the tumor microenvironment. We speculate that measurement of thrombin activity existing within malignant tissue may prove a useful means by which to identify tumors that might be most responsive to the new therapy.
Whether droplets are precoated with fibrinogen of human origin or of murine origin, they elicit in recipient mice a significant antibody response against the protein. Indeed, two of five mice treated with uncoated oil droplets developed measurable titers of antifibrinogen antibodies. Our observations and preliminary studies suggest such antibodies are of no obvious short term consequence in A/Jax mice bearing the ascites form of the TA3/St tumor; neither do they contribute to, nor do they detract from, the therapeutic benefit that derives from a single injection of docetaxel. But because even droplet-treated tumor-bearing A/Jax mice all succumb to tumor by 35 days, we are unable to make any claim regarding the long-term effects of the antibodies in those animals. It is conceivable such antibodies might limit the effectiveness of subsequent oil droplet treatments. Whereas that consideration was not apropos to the single treatment model used here by us (i.e., antibodies or not, droplets of docetaxel-loaded olive oil provided a benefit to survival significantly greater that that provided by Taxotere), it would be relevant to treatment regimens in which multiple doses of drug-loaded oil droplets were administered over time. We note anecdotally that the antifibrinogen antibody response of droplet-treated C57BL/6 mice is essentially the same as that of droplet-treated A/Jax mice.8 Importantly, two of nine C57BL/6 mice "cured" of an intraperitoneal form of B16F10 melanoma by treatment with fibrinogen-coated droplets of docetaxel-loaded olive oil (6) had no demonstrable antifibrinogen antibodies 1 year after treatment.8
To be sure, much still needs to be done to delineate both the benefits and limitations of the new docetaxel formulation, in particular, and of the delivery vehicle, in general. To date, we have used fibrinogen-coated droplets of docetaxel-loaded olive oil to treat only tumors that are, by intention, confined to the abdominal cavity. Whereas we suspect tumors confined to other closed spaces (e.g., the pleural cavity, pericardial sac, or brain case) will benefit similarly from treatment with the droplets, we have not yet tested that suspicion. Neither have we tested the efficacy of docetaxel-loaded droplets against tumors that either are located within a specific organ or are widely metastatic. We do know that, after their intravenous administration, fibrinogen-coated oil droplets are retained in organs of the reticuloendothelial system (3) . Thus, intravenous administration might be especially good for the delivery of droplets to tumors in organs that typically harbor metastatic disease. Regardless, we are now developing smaller versions of fibrinogen-coated oil droplets that might better circulate and percolate through tissues. We are also testing the suitability of fibrinogen-coated oil droplets for the delivery of a number of other lipophilic anticancer agents, both individually and in combination. Eventually, we hope to develop a single formulation that delivers several mechanistically dissimilar agents.
For many reasons, cancer patients are predisposed to thrombosis (19) , and thus they occasionally need to be treated with an anticoagulant or even a fibrinolytic agent. Our results suggest concurrent administration of such agents with fibrinogen-coated droplets of docetaxel-loaded olive oil might reduce the therapeutic efficacy of the droplets. On the other hand, if anticoagulants and fibrinolytics reduce the therapeutic efficacy of the droplets, then perhaps pro-coagulants and antifibrinolytics might improve efficacy. Clearly, before the full potential of fibrinogen-coated oil droplets as delivery vehicles for lipophilic anticancer agents can be realized, much more needs to be done to delineate the influence of coagulation-related medicinals on the new modality.
The use of docetaxel in its current clinical formulation is attended by several adverse side effects attributable to either the drug itself (e.g., fluid retention, neurotoxicity, musculoskeletal toxicity and neutropenia; ref. 20 ), or to the solvent system used in the drug’s commercial preparation (e.g., hypersensitivity; ref. 21 ). One would hope any new formulation of docetaxel would not only better target the drug to malignant tissue but would also be attended by fewer or less severe side effects. Although we addressed some toxicity issues in the studies presented here, we focused more on the anticancer efficacy of the new formulation and on understanding the basis of that efficacy than on adverse side effects. We hope in the near future to compare specific indices of toxicity (e.g., neutrophil count) after treatment of mice with docetaxel-loaded oil droplets to those same indices after treatment with Taxotere.
Aside from their ability to target tumors as sites of fibrin formation, fibrinogen-coated oil droplets (or other fibrinogen-coated microparticulates) might be ideally suited to delivering anticancer agents to malignancies for yet another reason. Work in one of our laboratories supports the hypothesis that macrophages transport particulate materials and even tumor cells in fibrinogen-dependent extracellular fashion (22) ,9 and one of us has proposed that metastasis is, at least in part, a manifestation of extracellular trafficking of tumor cells by macrophages (22 , 23) . If the macrophage-directed "traffic patterns" of particulate materials and metastatic tumor cells are the same, then it is not unreasonable to suppose anticancer agents delivered as/within fibrinogen-coated particulate materials might be exploited to target metastatic disease.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Requests for reprints: Gregory S. Retzinger, Pathology and Laboratory Medicine, University of Cincinnati, 231 Albert Sabin Way, Cincinnati, OH 45267-0529. Phone: 513-558-3447; 513-558-2289; E-mail: retzings{at}email.uc.edu
8 C. Einhaus and A. Perrotta, unpublished data. 
9 G. Retzinger, unpublished data.
Received 1/20/04; revised 6/24/04; accepted 7/ 7/04.
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), NS alone (n = 8); (•), NS and hirudin (n = 6); (
), Taxotere alone (n = 5); (
), BSA-coated droplets of docetaxel-loaded olive oil plus hirudin (n = 4); (
) human fibrinogen-coated droplets of docetaxel-loaded olive oil plus hirudin (n = 4); (
), uncoated droplets of docetaxel-loaded oil droplets plus hirudin (n = 4); and (
), human fibrinogen-coated droplets of docetaxel-loaded olive oil minus hirudin (n = 4). Whereas the three distinct groups of profiles are all significantly different from each other (P 
