Docetaxel-trastuzumab stealth immunoliposome: development and in vitro proof of concept studies in breast cancer
Authors Rodallec A, Brunel JM, Giacometti S, Maccario H, Correard F, Mas E, Orneto C, Savina A, Bouquet F, Lacarelle B, Ciccolini J, Fanciullino R
Received 13 January 2018
Accepted for publication 24 February 2018
Published 18 June 2018 Volume 2018:13 Pages 3451—3465
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Cristina Weinberg
Peer reviewer comments 3
Editor who approved publication: Dr Thomas J Webster
Anne Rodallec,1 Jean-Michel Brunel,2 Sarah Giacometti,1 Helene Maccario,3 Florian Correard,3 Eric Mas,3 Caroline Orneto,4 Ariel Savina,5 Fanny Bouquet,5 Bruno Lacarelle,1 Joseph Ciccolini,1 Raphaelle Fanciullino1
1SMARTc Unit, Pharmacokinetics Laboratory, CRCM UMR U1068 CNRS UMR 7258 Aix Marseille Université, Marseille, France; 2CRCM CNRS UMR 7258 Aix Marseille Université, Marseille, France; 3CRO2 UMR S_911 Aix Marseille Université, Marseille, France; 4Biopharmacy Laboratory, Aix Marseille Université, Marseille, France; 5Institut Roche, Boulogne Billancourt Cedex, France
Background: Trastuzumab plus docetaxel is a mainstay to treat HER2-positive breast cancers. However, developing nanoparticles could help to improve the efficacy/toxicity balance of this doublet by improving drug trafficking and delivery to tumors. This project aimed to develop an immunoliposome in breast cancer, combining docetaxel encapsulated in a stealth liposome engrafted with trastuzumab, and comparing its performances on human breast cancer cell lines with standard combination of docetaxel plus trastuzumab.
Methods: Several strategies to engraft trastuzumab to pegylated liposomes were tested. Immunoliposomes made of natural (antibody nanoconjugate-1 [ANC-1]) and synthetic lipids (ANC-2) were synthesized using standard thin film method and compared in size, morphology, docetaxel encapsulation, trastuzumab engraftment rates and stability. Antiproliferative activity was tested on human breast cancer models ranging from almost negative (MDA-MB-231), positive (MDA-MB-453) to overexpressing (SKBR3) HER2. Finally, cell uptake of ANC-1 was studied by electronic microscopy.
Results: ANC-1 showed a greater docetaxel encapsulation rate (73%±6% vs 53%±4%) and longer stability (up to 1 week) as compared with ANC-2. Both ANC presented particle size ≤150 nm and showed similar or higher in vitro antiproliferative activities than standard treatment, ANC-1 performing better than ANC-2. The IC50s for docetaxel combined to free trastuzumab were 8.7±4, 2±0.7 and 6±2 nM with MDA-MB-231, MDA-MB-453 and SKBR3, respectively. The IC50s for ANC-1 were 2.5±1, 1.8±0.6 and 3.4±0.8 nM and for ANC-2 were 1.8±0.3 nM, 2.8±0.8 nM and 6.8±1.8 nM with MDA-MB-231, MDA-MB-453 and SKBR3, respectively. Cellular uptake appeared to depend on HER2 expression, the higher the expression, the higher the uptake.
Conclusion: In vitro results suggest that higher antiproliferative efficacy and efficient drug delivery can be achieved in breast cancer models using nanoparticles.
Keywords: immunoliposomes, biopharmaceutical development, breast cancer, docetaxel, trastuzumab, HER2
Taxanes are a mainstay in the treatment of several solid tumors including breast cancer.1 By interfering with spindle dynamics, they stabilize microtubules and cause cell cycle arrest at the metaphase/anaphase, resulting in cell apoptosis. In vitro, docetaxel is generally twofold to fourfold more potent than paclitaxel.2 This greater tumor activity was confirmed at bedside in metastatic breast cancer.3 However, docetaxel patients display more severe hematological and non-hematological toxicities (eg, neutropenia, thrombocytopenia, stomatitis, asthenia) than paclitaxel patients.3 In addition, common drug-related toxicities are hypersensitivity reactions related to the solubilizing agents necessary to allow taxanes to be given as infusions.4,5 In this respect, incorporating taxanes into nanoparticles could help limiting treatment-induced toxicities, by skipping the use of solubilizing agents and sparing healthy tissues while better targeting tumor cells.6 Consequently, many liposomes and stealth liposomes have been developed, and have shown both in vitro and in vivo less toxicity with equivalent or higher efficacy against tumors.7,8 Similar better outcomes were evidenced when tested in clinical trials, either alone or in combination.9–11 However, unlike doxorubicin forms, no liposomal docetaxel has been approved yet in breast cancer. Therefore, although the first or second generation of liposomes displayed improved pharmacokinetics (ie, decreased clearance and higher tumor accumulation),12–14 further development of nanoparticles is still an ongoing story with taxanes. Thus, more sophisticated forms have been developed such as co-loaded liposomes (eg, docetaxel + palmitoyl ascorbate,15 paclitaxel + rapamycin,16 docetaxel + BCL-2 SiRNA17), triggered liposomes (eg, pH sensitive18 or thermosensitive19) and targeted liposomes. Many moieties (eg, small-molecule ligands, peptides20 and monoclonal antibodies) have been used over the last years to actively target cancer cells through different strategies, including targeting several receptors like folate receptors,21,22 integrin23 and transferrin.24,25 In the early 2010s, an immunoliposome of doxorubicin engrafted with anti-epidermal growth factor receptor cetuximab was developed and reached early Phase I clinical trials, although this combination had no clear application in breast cancer.26 However, this seminal study demonstrated that it was possible to target an external receptor expressed on cancer cell surface using a monoclonal antibody engrafted on a nanoparticle. Overexpressed in 20%–40% of breast cancers,27 human epidermal growth factor receptor-2 (HER2) is an attractive receptor likely to help targeting of nanoparticles loaded with cytotoxics. MM302, a stealth liposomal formulation of doxorubicin coated with an anti-HER2 antibody, showed appealing results when tested in early clinical studies,28 but unfortunately subsequent Phase II trial failed in confirming the promising Phase I results because of poor efficacy and futility.29 With MM302, targeting HER2 was achieved using a lab-synthesized anti-HER2 antibody. Of note, the approval of the anti-HER2 monoclonal antibody trastuzumab (Herceptin®), in the early 2000s has considerably improved the poor clinical outcome and survival of HER2+ breast cancer patients, when associated with docetaxel.29–31 Thus, developing directly a trastuzumab-coated liposomal taxane represents a promising and convenient strategy in breast cancer, rather than using home-made antibodies, as trastuzumab is a well-known and fully characterized antibody.32
In this study, we present the early development of such novel entity, combining stealth liposomal docetaxel with engrafted trastuzumab on its surface. Two formulations of liposomes with several engraftment techniques were tested: neutral formulation using phosphatidylcholine (antibody nanoconjugate-1 [ANC-1]) or positive formulation using 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP; ANC-2). Performances of the two resulting immunoliposomes were next compared in terms of physical characteristics, stability and antiproliferative efficacy in human breast cancer models varying in HER2 expression levels (Figure 1).
Figure 1 Formulation and testing of two different nanoparticles.
Materials and methods
Experiments were carried on three human breast cancer cell lines: SKBR3 (strong HER2 overexpression), MDA-MB-453 (HER2 overexpression) and MDA-MB-231 (HER2 mild expression). Cells were purchased from the American Type Culture Cell. Cells were cultured in RPMI supplemented with 10% FBS, 1% penicillin and 0.16% kanamycin and grown in a humidified CO2 incubator at 37°C. Cells were regularly authenticated on cell viability, morphology and doubling time.
Drugs and chemicals
Egg yolk phosphatidylcholine (PC), phosphatidylglycerol (PG), cholesterol (Chol), 1,2-distearoyl-sn-glycero-3-phosphoethanolamine and paclitaxel were purchased from Sigma (St-Quentin-Fallavier, France). 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[maleimide(polyethylene glycol)-2000] (Mal-PEG) and DOTAP were purchased from COGER (Paris, France). Docetaxel was purchased from VWR (Fontenay-sous-Bois, France). DIR, a fluorophore tag, was purchased from Caliper (Villebon-sur-Yvette, France). 2-Iminothiolane (Traut’s reagent) and Draq5 were purchased from Fisher Scientific (Illkirch-Graffenstaden, France). QuantiBRITE phycoerythrin (PE) and PE Mouse Anti-Human HER-2/neu were purchased from BD Biosciences (San Jose, CA, USA). Trastuzumab (Herceptin) was kindly given by Genentech (South San Francisco, CA, USA). All other reagents were of analytical grade.
Pegylated liposome preparation
Two compositions of liposomes were studied: Mal-PEG and docetaxel. Liposome-1 used PC, PG and Chol, whereas Liposome-2 used DOTAP with PC or Chol. Both compositions were synthesized using the classic thin-film method.33 Briefly, lipids were dissolved in methanol. Lipidic solution was further mixed with DIR as fluorophore when required. Methanol was then removed by rotary evaporation (Laborota 4003, Heidolph Instruments) at 38°C to avoid toxicity. After 30 minutes, a thin lipid film was obtained. To remove the residual solvent, lipid film was dried under stream of nitrogen for 2 hours at room temperature. The film was then hydrated with a 5% vol/vol glucose solution, and MLV liposomes were obtained. Several strategies were performed to reduce and homogenize liposomes in size. Extrusion through 400, 200, 100 and 80 nm polycarbonate pore membranes (Nuclepore, Whatman France) using a LipoFast LF-50 or alternatively 20 kHz sonication on ice for 5 minutes at 4°C using a Branson Sonifier 250 sonic probe were tested.34,35
Pegylated immunoliposome preparation: antibody engraftment
Trastuzumab engraftment was performed from previously obtained Liposome-1 and Liposome-2, generating immunoliposomes made of PC (ie, ANC-1) or DOTAP ± PC or Chol (ie, ANC-2). In addition, two different engraftment strategies36 were tested. Strategy A targeting the amine function relied on increasing the pH of the liposome solution with the addition of NaOH. Two alternative modalities of NaOH addition were further tested: during the hydration step of the lipid film and after the extrusion step. Once extruding pH was >8.5 for liposome solution, trastuzumab was added in 1:65 molar ratio (trastuzumab: Mal-PEG). The mixture was then kept under constant overnight shaking. Alternatively, strategy B targeting the thiol function36–38 required a preliminary step of trastuzumab thiolation. To this end, trastuzumab was first dissolved in a 0.1 M sodium phosphate-buffer saline (PBS), pH 8.0, containing 5 mM ethylenediaminetetraacetic acid and mixed under constant shaking, for 2 hours at room temperature with a Traut’s reagent solution at 1:10 molar ratio (Traut’s: trastuzumab). Thiolated trastuzumab was then directly mixed with the pegylated liposomes at 1:127 molar ratio (trastuzumab: MAL-PEG). The mixture was kept under constant shaking at 4°C overnight. For both strategies, unbound trastuzumab and free docetaxel were removed from the liposomal solution using 6,000 g centrifugation on MWCO 300 KDa vivaspins (VWR).39,40
Size and polydispersity study
Size and polydispersity index (PDI) were measured by light scattering (LDS). Liposomes and immunoliposomes were diluted in a PBS solution and then analyzed by a Zeta sizer Nano S (Malvern Instruments, Malvern, UK). Liposomal preparations were considered unimodal for a PDI <0.2.41,42
Docetaxel encapsulation rate and entrapment efficiency
Docetaxel concentrations were measured using a validated high pressure liquid chromatography-UV method43 after liquid/liquid extraction and using a C18 column (25 cm×4.6 mm, 5 μm, Waters, Guyancourt, France). The mobile phase was composed of 53% of ammonium acetate buffer (35 nM, pH 5) and 47% of acetonitrile. Samples were eluted at a constant flow rate of 1.8 mL/min with UV detection (227 nm). Analysis was performed on an Agilent 1100 liquid chromatography system. Data were acquired and analyzed using Chemstation software (Agilent, Les Ulis, France). Docetaxel and paclitaxel typical retention times were 11 and 13.5 minutes, respectively. Encapsulation rate for docetaxel was calculated using the following formula:
Entrapment efficiency for docetaxel was calculated using the following formula:
Trastuzumab engraftment rate
Sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis was performed to show the presence and integrity of engrafted trastuzumab on liposome using polyacrylamide 10% gels, with a constant voltage of 100 V. The running buffer was composed of Tris/glycine/SDS. The gel was stained with Coomassie blue and rinsed overnight prior analysis. Additionally, trastuzumab engraftment rate was indirectly measured by the Bradford assay,44 using thiolated trastuzumab as the reference standard.
Electronic microscopy analysis
Liposomes were diluted in PBS and dropped on a copper grid. After 15 minutes, they were stained for 5 minutes with 5% uranyl acetate or 2% osmium tetroxide before being dried out overnight at room temperature. The grid was then observed at 80 kV using transmission electron microscopy (JEM-1410; JEOL Ltd., Tokyo, Japan) coupled with a Megaview III camera (Soft Imaging System, Münster, Germany).
Stability studies were performed on several storage conditions (ie, 20% diluted ANC kept at −20°C, concentrated and 20% diluted ANC kept at 4°C and 20% diluted ANC kept at 25°C), always protected from light. Liposome size, PDI, docetaxel leakage and persistence of the engrafted trastuzumab were evaluated weekly for a month, then bimonthly for up to 46 days.
Quantification of HER2 on cells
As previously described,45 QuantiBRITE PE (BD Biosciences) was used to estimate the absolute number of HER2 on cell membranes. About 100,000 cells of SKBR3, MDA-MB-453 or MDA-MB-231 were incubated under saturated conditions with PE Mouse Anti-Human HER-2/neu (BD Biosciences) for 30 minutes at 4°C before being rinsed with PBS. IgG2a-PE anti-mouse antibodies (Fisher Scientific) were used for isotopic control. Analysis was then immediately performed on Gallios Beckman Coulter. Assuming our anti-HER-2 PE antibody has a 1:1 fluorochrome: antibody ratio, we determined PE median fluorescence intensity (MFI) for all cell lines and reported it on a log-log graph with MFI vs PE molecules, after subtracting isotopic control MFI. Of note, to avoid PE signal saturation, adjustment of QuantiBRITE in low sensitivity conditions was performed on SKBR3 cells.
In vitro antiproliferative activity
SKBR3, MDA-MB-453 and MDA-MB-231 were seeded on a monolayer 96-well plate at a density of about 6,000 cells/well for 24 hours before the experiment begins. After overnight attachment, cells were exposed continuously for 72 hours to docetaxel (0.01–100 nM) and trastuzumab (0.02–200 pM). Different conditions were tested: free docetaxel, free trastuzumab, free drugs (docetaxel plus free trastuzumab), Liposome-1 plus free trastuzumab, Liposome-2 plus free trastuzumab, ANC-1 and ANC-2. Cell viability was determined using the MTT assay and spectrophotometric reading at 550 nm (PowerWave XS2; BioTek, Saint-Jean-de-Védas, France).
In vitro cellular uptake
SKBR3, MDA-MB-453 and MDA-MB-231 were seeded on Lab-Tek chamber slides (Nunc, Roskilde, Denmark) at a density of about 20,000 cells/well for 24 hours before the experiment begins. After overnight attachment, cells were exposed continuously for 6 hours to DIR-labeled ANC-1 and labeled with Draq5. Next, cells were fixed with ice-cold methanol and incubated for 5 minutes at −20°C before being rinsed with PBS. Cellular uptake was observed using confocal microscopy (TCS SP2 Leica) coupled to a digital camera.
In vitro experiment was performed at least in triplicate and data were represented as mean ± SD or ± standard error of the mean. Statistical analyses were performed on MedCalc 17.2.1. Software (MedCalc, Acacialaan, Belgium).
Size and polydispersity
ANC-1 and ANC-2 displayed 140±3.4 and 150±5 nm diameters, respectively. PDI was found to be much lower after extrusion as compared with sonication (ie, 0.11±0.02 vs 0.39±0.001; p<0.001, Student’s t-test) and subsequent batches of liposomes were prepared by extrusion only (Table 1). With increasing number of extrusion cycles, both PDI and liposome size decreased (Table 1). Shifting from 4 to 6 extrusion cycles on 100 nm pore membranes led to 17% decrease in size with a 1.44-fold reduction in PDI. Use of 80 nm pore membrane led to a further 22% size reduction, without affecting PDI (Table 1). No significant difference in size was observed when adding upfront extrusions on 400 nm pore membrane (Table 1). Trastuzumab engraftment increased diameters of ANC-1 and ANC-2 by 9±4 and 22±2 nm, respectively (Table 2).
Table 1 Summary of the different extrusion conditions tested on Liposome-1a
Docetaxel encapsulation rate and entrapment efficiency
Results of docetaxel encapsulation rate for Liposome-1 and Liposome-2 are summarized in Tables 3 and 4, respectively. Sonicated liposomes showed higher encapsulation rates as compared with liposomes obtained after extrusion (ie, 76%±11% vs 35%±19%; p=0.037, t-test). Adding PG to Liposome-1 composition increased docetaxel encapsulation rate from 35%±19% to 63%±18% (Table 3), with an optimal molar ratio of 50:19:15:1 (PC:Chol:PG:Mal-PEG). In these conditions, the 1.9% docetaxel: lipid molar ratio achieved the highest encapsulation rate as compared with 1.8% and 2.0% molar ratios (ie, 85%±2% vs 70%±19% vs 63%±18%, respectively, p=0.244, ANOVA test, Table 3). Adding PC to Liposome-2 composition increased the encapsulation rate from 13%±2% to 72%±1%, a value higher than the one obtained with DOTAP/Chol liposomes (59%±8%, p=0.032, t-test, Table 4). Molar ratio of 50:19:15:1%–1.9% (PC:Chol:PG:Mal-PEG-docetaxel:lipid) for Liposome-1 and molar ratio of 18:17:1%–5% (DOTAP:PC:Mal-PEG-docetaxel:lipid) for Liposome-2 were selected to further engraft trastuzumab and to generate ANC-1 and ANC-2, respectively. Their formulation and characteristics are summarized in Table 2. ANC-1 and ANC-2 exhibited docetaxel encapsulation rate of 73%±6% and 53%±4% respectively (p=0.003, t-test, Table 2). Docetaxel entrapment efficiency was found to be significantly higher than encapsulation rates (ie, >90% for ANC-1 and >75% for ANC-2, Table 2).
Trastuzumab engraftment rate
The two engraftment strategies (ie, targeting the amine [strategy A] and the thiol [strategy B] functions) were tested on Liposome-1 only. Electrophoresis gel was used to confirm trastuzumab engraftment, as shown in Figure S1. As previously described,32 engrafted trastuzumab showed a slightly larger molecular weight (S1-A5), compared to the native form (S1-A2 and A3). However, strategy A did not present this shift (S1-A7), suggesting that this method did not allow proper engraftment on the liposomes and therefore was not tested on Liposome-2. On Liposome-1, strategy B did present this shift (S1-B5 and B3) and was also validated on Liposome-2 (S1-B5). Trastuzumab engraftment rate was indirectly measured by Bradford assay and found to be 31%±6%, and 32%±2% for ANC-1 and ANC-2, respectively.
Electronic microscopy studies
ANC-1 (Figure S2) and ANC-2 (Figure S3) showed spherical shapes of homogeneous size. Upon transmission electron microscopy imaging, mean diameters were 129±10 nm and 144±31 nm for ANC-1 and ANC-2, respectively. Several lipid bilayers were also observed on Liposome-1 examined before extrusion step (Figure S4).
When monitoring docetaxel encapsulation rate over time (Figure 2), no significant differences were found between the storage conditions (ie, −20°C, 4°C, 25°C). ANC-1 and ANC-2 showed docetaxel leakage, with a decrease in docetaxel of 19%±20% and 48%±19% per week, respectively (p<0.001, t-test). Size was regularly evaluated as well, until docetaxel reached 0% (ie, 45 days for ANC-1, Figure S5, and 15 days for ANC-2, data not shown). No significant difference was observed in size between ANC-1 and ANC-2. When diluted or concentrated at 4°C or diluted at 25°C, size was steady over time (Figure S5). Only ANC kept at −20°C led to an increase in diameter over time. Within a week, size increased from 140±3 to 220±25 nm for ANC-1 (p=0.004, t-test) and from 158±13 to 217±14 nm for ANC-2 (p=0.04, t-test) before being stabilized. Trastuzumab engraftment was persistent after 45 days for ANC-1 (Figure S1-B7). Similar results were found with ANC-2 (data not shown).
Quantification of HER2 on cells
Flow cytometry analysis allowed measuring the expression of HER2 on the surface of every cell lines, with marked differences (Figure 3). Of note, it was possible to detect and to quantify HER2 in MDA-MB-231 cells, despite their status of HER2-negative canonical model. SKBR3, MDA-MB-453 and MDA-MB-231 were found to express 1,117.103±17.103, 215.103±37.103 and 5.103±0.3.103 HER2 receptors per cell, respectively (p<0.001, one-way ANOVA, Figure 2).
Figure 3 Quantification of HER2 using QuantiBRITE kit in standard conditions on MDA-MB-231 and MDA-MB-453 (A) and in lower intensity conditions on SKBR3 (B).
In vitro antiproliferative activity
Results of cytotoxicity studies are summarized in Figure 4 (MDA-MB-231), Figure 4 (MDA-MB-453) and Figure 5 (SKBR3). As expected, both empty liposomes and single-agent trastuzumab46 showed no antiproliferative activity on our cell models (data not shown). The IC50s for docetaxel combined to free trastuzumab were 8.7±4, 2±0.7 and 6±2 nM with MDA-MB-231, MDA-MB-453 and SKBR3, respectively. The IC50s for ANC-1 were 2.5±1, 1.8±0.6 and 3.4±0.8 nM and for ANC-2 were 1.8±0.3, 2.8±0.8 and 6.8±1.8 nM with MDA-MB-231, MDA-MB-453 and SKBR3, respectively. On MDA-MB-231 cells, reaching IC50 was achieved with 71% lower dose (p=0.029, t-test) as compared with free drugs for ANC-1 and 79% lower dose (p=0.043, t-test) for ANC-2 (Figure 5). For MDA-MB-453 and SKBR3, IC50 were reached using 8% (p=0.799, t-test) and 44% (p=0.2, Mann–Whitney test) lower dose, respectively, for ANC-1 (Figure 6). Conversely with ANC-2, 38% and 13% higher dose were required to reach the IC50 with MDA-MB-453 and SKBR3 as compared with free drugs (Figure 6). Engrafting trastuzumab to liposomes (ie, ANC vs liposome) did not improve efficacy on in vitro 2D models, regardless of the cell lines (Figure 7).
In vitro cellular uptake
After 6 hours, cellular uptake of ANC-1 was observed in all cell models. ANC-1 was primarily localized around cell nucleus. Upon observation, ANC-1 seemed to better accumulate in SKBR3 than in MDA-MB-453, and in MDA-MB-453 than in MDA-MB-231 (Figure 8A–C). Although not quantitative, a trend toward a relationship between HER2 expression rate and ANC-1 cellular uptake was observed.
Figure 8 Confocal microscopy observations of ANC-1 uptake on SKBR3 (A), MDA-MB-453 (B) and MDA-MB-231 (C) cells, after 6 hour exposition.
Improving drug delivery is a promising strategy to optimize anticancer drug efficacy while limiting treatment-related toxicities.47 Nanoparticles can accumulate in tumor surroundings via the enhanced permeation and retention (EPR) effect, helping cytotoxics to better trafficking to tumor tissues eventually.34 Here, we have developed novel and innovative immunoliposomes coupling docetaxel and trastuzumab to be used in breast cancer models. Simple and rapid thin-film method was used to synthesize stealth liposomes of docetaxel, making the production of the nanoparticles simple, cheap and reliable throughout time. Trastuzumab, used as a targeting agent towards HER2, was best engrafted via sulfhydryl groups on maleimide polyethylene glycol. Several formulations were tested and optimized, focusing on docetaxel encapsulation rate, size and polydispersity as endpoints. Required size has to be below 200 nm indeed to benefit from passive targeting through the EPR effect,33,34 the smaller the liposome, the higher specificity.48 Here, extrusion and sonication techniques were both tested to reduce liposome diameter. Extrusion generated a loss of volume, affecting docetaxel encapsulation rate when compared to sonication; however, extrusion was finally preferred because of better homogeneity in size. Two extrusion cycles on 400, 100, and 80 nm pore membranes were considered as the best compromise between adequate size, PDI and encapsulation rate. ANC-1 and ANC-2 displayed a size of 140±3.4 and 150±5 nm, respectively. Engrafting trastuzumab slightly reduced docetaxel encapsulation rates. This decrease could be explained by weakening of liposomes during stirring. Finally, ANC-1 presented a 20%±10% higher docetaxel encapsulation rate than ANC-2. The engraftment rate was similar for both compositions and in line with previous works.40 Stability studies showed that shelf conditions could be indistinctively 4°C or 25°C, protected from light, for up to 1 week. ANC size remained steady with no signs of coalescence. However docetaxel concentration decreased rapidly (ie, 19% decrease after 1 week for ANC-1). ANC-2 was found to be even less stable, probably because of the absence of cholesterol49 resulting in higher docetaxel leakage. Consequently, extemporaneous preparation was required to perform in vitro studies. In the future, lyophilization could be an interesting strategy to fix the issue of storage and drug leakage,12 although preliminary studies suggest that it may lead to an increase in size (data not shown). Future plans include use of sugar derivatives as cryoprotector, as a means to stabilize the nanoparticle during the lyophilization phase.
Human MDA-MB-231, MDA-MB-453 and SKBR3 cell lines were chosen as cancer model because of marked variations in HER2 expression. Of note, although MDA-MB-231 are usually presented as a canonical triple negative model, we were able to detect HER2 expression with this cell line, which is markedly lower as compared with MDA-MB-453 and SKBR3 cells. As expected, empty liposomes and trastuzumab alone did not show any antiproliferative effect. Combining docetaxel with trastuzumab led to a significant increase of sensitivity for MDA-MB-453 cells when compared to free docetaxel only. MDA-MB-231 (HER2±) and MDA-MB-453 (HER2+) were found to be the most resistant and the most sensitive to free drugs, respectively, an observation in line with differences in HER2 expression between these cells. Encapsulating docetaxel in ANC-1 led to an increased efficacy on MDA-MB-231, SKBR3 and MDA-MB-453. Encapsulating docetaxel in ANC-2 led to an improved efficacy on MDA-MB-231 only. Overall, both liposomal docetaxel and ANC showed improved efficacy in resistant tumor cells, suggesting a better ability to circumvent drug resistance using nanoparticles. No significant difference was observed between Liposome-1 plus free trastuzumab and Liposome-2 plus free trastuzumab when compared to ANC-1 and ANC-2, suggesting that 2D antiproliferative experiments as we performed may not properly address the issue of immunoliposomes efficacy.7 Indeed, because monoclonal antibodies barely diffuse within tissues and tumors, the benefit from engrafting trastuzumab to a highly lipophilic nanoparticle can be hardly evidenced using models of monolayer cancer cells. Here, the expected benefit with immunoliposomes is based upon the hypothesis that when engrafted to a liposome, the antibody will more easily penetrate deep into the tumor mass, rather than being restricted to hitting targets of the external layer of cells. Spheroids or organoids should therefore be used in the future to better compare the performances of immunoliposomes with that of standard cytotoxics + monoclonal antibody combination. Because of its specific composition, ANC-1 exhibited better performances in terms of size, encapsulation rates, stability and in vitro activity as compared with ANC-2. Therefore, ANC-1 only was selected for further analysis of cellular uptake. Interestingly, cellular uptake was different depending on the cell line, an observation in line with measurement of HER2 expression between MDA-MB-231, MDA-MB-453 and SKBR3 breast cancer cells, the higher the expression, the higher the uptake. Differences in cell uptake are not consistent with differences in efficacy observed during antiproliferative activity testing, but this discrepancy could be due to differences in timing between uptake studies (6H) and the endpoint of efficacy studies (72H). Overall, the early data we generated indicate that redesigning an approved combo (ie, trastuzumab + docetaxel administrated separately) as a single nanoparticle is feasible and exhibits promising antiproliferative efficacy in a variety of cancer models. Targeting HER2+ breast cancer with nanomedicine is certainly not new and several studies with polymeric micelles encapsulating HSP90 inhibitor, paclitaxel and trastuzumab have shown excellent efficacy, both in vitro and in tumor-bearing mice.48 Of note, HSP inhibition could further help HER2-targeting carriers to better trafficking inside cancer cells through extra-lysosomal targeting, thus enabling a better internalization of the nanoparticle-HER2 complex.49 The extent of adding a HSP inhibitor to the design of our ANC will have to be evaluated to further optimize drug delivery to HER2+ cancer cells.
In this work, we demonstrated the feasibility of making 3rd generation liposomes in breast cancer, using a cheap and rapid process. Development showed that composition of the liposomes has a strong impact on subsequent characteristics and performance. Although preliminary and still showing several caveats (eg, stability limited to 1 week) that require to be addressed, in vitro results are promising and suggest that delivering cytotoxics plus biologics could be optimized when administered as immunoliposomes, rather than as free drugs.
The authors would like to thank the platform Amuticyt (VRCM) de la faculté de Pharmacie La Timone and the Service Commun de Microscopie Électronique de la Faculté de Médecine La Timone for their technical expertise. The authors would also like to thank the Ligue Contre le Cancer who generously provided a grant to AR. Additionally, we thank the French Institut Roche who partly supported this study and Genentech who kindly provided trastuzumab.
AR, RF, JC, SG, JMB, HM, FC, EM and CO performed the bench experiments. AR, RF and JC performed statistical analyses. AR, RF, BL, AS, FB and JC wrote the manuscript. All authors contributed toward data analysis, drafting and revising the paper and agree to be accountable for all aspects of the work.
AS and FB are members of the Institut Roche, a joint-institute from Roche Laboratories that commercializes trastuzumab and has partly funded this study. JC and RF received fees as board members of Roche. The authors report no other conflicts of interest in this work.
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Figure S2 TEM observations of ANC-1 treated with osmium tetroxide (A and B) and uranyl acetate (C).
Figure S3 TEM observations of ANC-2 treated with osmium tetroxide.
Figure S4 TEM observations of liposome-1 before extrusion.
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