Development of theranostics albumin auristatin conjugates for combining chemotherapy with boron neutron capture therapy

doi:10.21203/rs.3.rs-3589431/v1

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Development of theranostics albumin auristatin conjugates for combining chemotherapy with boron neutron capture therapy

https://doi.org/10.21203/rs.3.rs-3589431/v1

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Combining boron neutron capture therapy with chemotherapy can provide good therapy efficacy and is of great relevance today. In this study, we focused on serum albumin, a well-known drug delivery system, and developed homocysteine-functionalized boron albumin conjugate with chemotherapeutic molecules (monomethyl auristatin E, MMAE and auristatin F, MMAF). The new N-acylated homocysteine thiolactone bearing a cobalt bis(dicarbollide) derivative was used to create the fluorophore-albumin based construct. We report on the synthesis of a fluorophore-labeled boron-homocystamide conjugates of human serum albumin and their use in thiol-‘click’ chemistry to prepare a novel multifunctional constructs with the antitubulin agents MMAE or MMAF. We demonstrate that boron-equipped albumin conjugate with MMAE was more potent than MMAF conjugate, in the killing tumor cells. The half-maximal inhibitory concentration (IC₅₀) of the designed theranostics was not less than 0.034 µM relative to T98G glioma cells with the correlation coefficient not less than R = 0.88, and not less than 0.97 µM relative U 87 glioma cells with the correlation coefficient not less than R = 0.71.

Drug Discovery, Design, & Development

Drug Delivery

Organic Chemistry

Boronated albumin theranostic conjugates

Monomethyl auristatins

Boron neutron capture therapy

Boron delivery agents

Monomethyl auristatins E and F are potent derivatives of the natural product dolostatin 10 that inhibit tubulin polymerization in dividing cells and thereby induce apoptosis [1,2]. Since the original discovery of dolastatin 10 in 1987, the auristatins have attracted considerable interest due to their exceptional cytotoxicity, which is roughly 100–1000 times higher than that of doxorubicin, a previously often employed anticancer therapeutic [3]. Additionally, auristatins function as the vascular disrupting agents and damage the established tumor vessels. While this potential was intriguing to the scientific community, the high toxicity imposed severe constraints, which limited the practical applicability of auristatins for decades.

It was eventually discovered that auristatins are of great value as payloads in antibody drug conjugates (ADCs), which led to the FDA-approved ADC brentuximab vedotin (Seattle Genetics) [2]. Seattle Genetics has pioneered the selective delivery of auristatins to tumor cells by further modifying them to suitable analogues, including di-desmethylauristatin E and monomethylauristatin E, and conjugating them to tumor-targeting antibodies in the Fc region through a linker.

Currently, over 30 ADCs in clinical trials employ auristatins as payloads, and there is a great interest in the research community, both on academic and industrial sides, to further study these analogues [4]. However, in practice, the auristatin ADCs do display a number of side effects such as neutropenia, neuropathy, thrombocytopenia, and ocular toxicity [5]. A consequence of the adverse effects may be the reason why these ADCs are, for the most part, not currently considered as the primary cancer treatment options. Moreover, the subclonal diversity of the tumor cells in a single patient regarding their genetic, epigenetic, and phenotypic properties, known as intratumor heterogeneity, fundamentally restricts active tumor targeting to a limited population of tumor cells expressing the target molecule. In addition, their complex synthetic chemistry hindering industrial-scale manufacturing is a formidable challenge for clinical translation.

We are interested in this class of molecules as they could also feed our ongoing program in the development of prodrugs of the human serum albumin [6,7]. Human serum albumin (HSA) has been well established as a platform for various diagnostic and therapeutic applications [8,9]. HSA has been successfully used clinically as a noncovalent carrier for insulin (e.g., Levemir), GLP-1(e.g., Liraglutine), and paclitaxel (e.g., Abraxane). As an excellent drug delivery carrier, albumin has been widely applied in the development of anticancer drugs [10]. It was discovered that auristatins are of great value as payloads in albumin drug conjugates [11-17]. It was demonstrated that auristatin-HSA conjugates exert potent activities on cancer cell. Until now, the latest research progress of albumin drug conjugates was that of Xinquan Liu et al. [11]. They tried to replace the antibody of ADC (antibody drug conjugate): Adcetris (CD30-VC-MMAE, VC-MMAE is the most successful linker payload in ADC) with albumin. The obtained conjugate HSA-VC-MMAE was broad-spectrum compared to Adcetris and could avoid the need for high antigen expression. However, to achieve similar in vivo potency, Adcetris (MMAE: 0.018 mg/kg) was significantly greater than conjugate HSA-VC-MMAE (Conjugate: 47 mg/kg, MMAE:0.5 mg/kg). In summary, although albumin as a broad-spectrum drug carrier could obviously reduce the times of administration, its weak efficacy still limits its use.

Current anticancer research shows that a combination of multiple treatment methods can greatly improve the killing of tumor cells. It is speculated that combining chemotherapy with boron neutron capture therapy (BNCT) can provide good therapy efficacy and is of great relevance today [18,19]. BNCT, in which drugs containing enriched boron are accumulated in tumor cells followed by their neutron beam radiation offers an advantage over conventional chemo- and radiotherapies as it selectively targets tumor cells. Currently, some research groups developed maleimide-functionalized closo-dodecaborate and aimed to conjugate it to albumin [20-24]. Conjugation of albumin with undecahydro-closo-dodecaborate did not significantly affect cell viability in the absence of irradiation, as compared with the unmodified protein. However, neutron capture by this boron-containing albumin decreased the tumor cell survival. It was found that dodecaborated albumin conjugates induces an efficient boron neutron capture reaction because the albumin contained in conjugate is retained in the tumor and has a considerable potential to become an effective delivery system for BNCT in treating high-grade gliomas [25].

In this study, we reported on the synthesis of a fluorophore-labeled boron-homocystamide conjugates of albumin and their use in thiol-‘click’ chemistry to prepare a novel multifunctional constructs with the antitubulin agents (MMAE and MMAF) for combining chemotherapy with BNCT. We studied the tumor cell killing properties of the theranostics albumin auristatin conjugates in human glioma cells compared with boron-albumin conjugate and free MMAE or MMAF.

Chemicals, reagents, and facilities

The human glioblastoma T98G and U87 cell lines were received from the Russian cell culture collection (Russian Branch of the ETCS, St. Petersburg, Russia).

Unless otherwise indicated, all of the starting materials and solvents were obtained from commercial suppliers at the highest grade available and used without further purification. All reactions were monitored by thin layer chromatography (TLC) on DC-Alufolien Kieselgel 60 F254 plates (Merck, Germany) with fluorescence F-254 and visualized with UV light. Column chromatography was carried out on silica gel (Acros Organics, 0,060 − 0,200 mm).

Drug-linker conjugates (mc-vc-pab-MMAE and mc-vc-pab-MMAF) were provided by Pharmaceutical company Suzhou Jianhua Co., Ltd. (Suzhou, China). D,L-Homocysteine thiolactone hydrochloride (DL-HTL × HCl) hydrochloride and the human serum albumin (HSA) was obtained from Sigma–Aldrich Chem. Co. (St. Louis, MO, USA). The product number of HSA used was A3782.

The concentrations of albumin solutions were determined by absorption at 278 nm, pH 7.4, using the molar extinction coefficient ε = 3.7 × 10⁴ M^-1cm^-1 [26].

Electronic absorption spectra were acquired on a UV-1800 spectrometer (Shimadzu, Japan).

IR spectra were recorded in the range 4000–400 cm^–1 using a Genesys 64 v/vis spectrometer.

¹H NMR, ¹³C NMR and ¹⁹F NMR spectra were recorded on AV-300, AV-400, AV-600 NMR spectrometer (Bruker, Germany). The spectra were detected at 25°C in 5 mm NMR sample tubes. D₂O (δ 3.8 ppm), acetone-d6 (δ 2.05 ppm) was used as an external reference for chemical shifts in ¹H NMR spectra. Acetone-d6 (δ 206.35 ppm) was used as an external reference for chemical shifts in ¹³C NMR spectra. Chemical shifts (δ) are reported in parts per million (ppm).

ESI mass spectra were registered on Agilent ESI MSD XCT Ion Trap (Agilent Technologies, Santa Clara, CA, USA) in positive or negative mode at The Joint Center for genomic, proteomic and metabolomics studies (ICBFM SB RAS, Russia).

Mass spectra of proteins and peptides were recorded on Bruker Autoflex Speed (Bruker Daltonics, Germany) MALDI-ToF mass spectrometer in a positive linear mode. A smartbeam-II laser was used. 2,5-Dihydroxyacetophenone (2,5-DHAP) was used as a matrix. Protein samples were desalted by ZipTip C4 pipette tips. A 2 µL of the protein sample solution was mixed with 2 µL of a 2% TFA (trifluoroacetic acid). To the latter solution 2 µL of the matrix (2,5-DHAP) was added. The mixture was pipetted up and down until the crystallization starts. Mass spectra were obtained by averaging 3,000 laser shots. External calibration was provided by [M + H]⁺ HSA at m/z 66.5 kDa.

SDS–PAGE. Human serum albumin conjugates were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis using 7% PAAG under Laemmli condition without the addition of DTT or DTT with subsequent Coomassie Brilliant Blue (BioRad) staining.

Low molecular weight materials (MW< 3 kDa) were removed from solutions of polymer conjugates by centrifugal filtration using Centricon concentrators with a MWCO of 3 kDa (Amicon Centriprep YM30, Millipore, Bedford, MA).

Synthesis of the homocysteine thiolactone containing bis(dicarbollide) complex of cobalt (III)

The synthetic route for the homocysteine thiolactone containing bis(dicarbollide) complex of cobalt (III) is shown in Scheme 1. The original mass spectrometry and NMR spectral details of the synthesized compounds are provided in Fig. S1 and S2.

Compound 2 was synthesized using previously reported experimental protocols [27]. One of the convenient methods for the functionalization of the bis(dicarbollide) complex of cobalt (III) is the preparation of its oxonium derivative (3) entering into a nucleophilic substitution reaction. The resulting nucleophilic attack product (4) contains a linker for further modification. Compound 3 was synthesized according to the adapted procedure [28]. The interaction of compound 3 with p-hydroxybenzoic acid methyl ester leads to the formation of compound 6 according to the procedure [29]. Then, the compound 4 was subjected to basic hydrolysis to give the compound 5, which was further activated with pentafluorophenol in the presence of dicyclohexylcarbodiimide to produce compound 6 at 77% yield. Detailed synthetic procedures and spectroscopic data of synthesized compound are given in Supporting Information.

Synthesis of N-substituted boron-homocysteine thiolactone K[3,3’-Co(B₉C₂H₁₁)(8-B₉C₂H₁₁OCH₂CH₂OCH₂CH₂OC₆H₄CONH-C₄H₅SO)] (compound 7, Scheme 1)

A solution of DL-HTL × HCl in DMF (0.1 mL, 0.065 mmol) was mixed with 0.015 mL of DIPEA and added to a DMF solution of the compound 6 (0.2 mL, 0,059 mmol). The resulting mixture was heated to 60°C for 4 hours with a reverse refrigerator. After that, solvent was evaporated on a rotary evaporator and 0.35 mL of ethyl acetate was added. The organic phase was washed with water solution of citric acid (10%, 2 × 0.11 mL) and then by water solution of potassium carbonate (10%, 2 × 0.12 mL). The organic phase was dried with dehydrated sodium sulfate and the solvent was evaporated on a rotary evaporator. The resulting compound was purified by column chromatography on silica gel (eluent: CH₂Cl₂/acetone 10:16 by volume) giving 0.026 g of an orange oil.

The yield of the product 7 65%. IR (KBr, cm^-1): 3400 ν(N-H); 2990, 2910, 2840 ν(C-H); 2550 ν(B-H); 1650 ν(C = O); 1620 δ(N-H); 1500, 1450 ν(C-N); 1230, 1120, 1090 ν(O-C-O)_asym. UV-vis (CH₂Cl₂): λ_max 246 nm (ε = (2.63 ± 0.02) × 10⁵), λ_max 448 nm (ε = (4.10 ± 0.01) × 10²). ¹H NMR (Acetone-d6, δ, ppm): 7.88 (2H, d, H-9); 7.02 (2Н, d, H-8); 4.94 (1H, m, H-12); 4.28 (4Н, s, H-1, H-2); 4.19 3.83 3.58 2.87 (8H, t, H-6, H-5, H-4, H-3); 3.49 (1H, m, H-14α); 3.35 (1H, m, H-14β); 2.66 (1H, m, H-13α), 2.34 (1H, m, H-13β). ¹³С NMR (Acetone-d6, δ, ppm): 205.4 (1C, s, C-15); 167.3 (1C, s, C-11); 162.8 (1C, s, C-7); 130.0 (1C, s, C-9); 127.2 (1C, s, C-10); 115.1 (1C, s, C-8); 72.9 (1C, s, C-6); 70.0 (1C, s, C-5); 69.3 (1C, s, C-3); 68.6 (1C, s, C-4); 59.7(1C, s, C-12); 55.2 (1C, s, C-2); 47.3 (1C, s, C-1); 31.4 (1C, s, C-14); 27.5 (1C, s, C-13). Mass spectrometry (ESI, negative) m/z: calculated for 647.1; measured value MW 646.8.

Synthesis and characterization of multifunctional human serum albumin-therapeutic conjugates

HSA-Cy5. The synthesis of HSA-Cy5 was adapted from Chubarov et al. [30].

HSACy5HcyCo(B ₉ C ₂ H ₁₁ ) ₂. A solution of HSA-Cy5 in PBS buffer (2.235 mL, 8.4 × 10^− 4 M, 1.88 µmol) was mixed with Co(B₉C₂H₁₁)₂-HTL dissolved in DMSO (118 µL and 12.2 µmol). Molar ratio Co(B₉C₂H₁₁)₂-HT / HSA was 6.5 and a volume ratio DMSO / PBS in the reaction mixture was 0.05. The reaction was carried out for 42 h at 37° C. Purification of the final conjugate was performed using centricons (Amicon Centriprep YM30, Millipore, Bedford, MA) that pass molecules with a molecular weight of less than 3,000 Da. For washing, 10% (by volume) DMSO in PBS, 10 volumes of the reaction mixture, and then PBS, 10 volumes of the reaction mixture were used. The yield of HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ was ~ 66%. UV-vis (PBS buffer, pH 7.4): λ_max 278 nm (ε = (8.27 ± 0.1) × 10⁴), λ_max 646 nm (ε = (6.64 ± 0.1) × 10⁴). Mass spectrometry (MALDI-TOF) m/z: measured average MW for HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ is 67,982 Da corresponds to two residues of HcyCo(B₉C₂H₁₁)₂ per one molecule of HSA (calculated MW for HcyCo(B₉C₂H₁₁)₂ 647 Da). Inductively coupled plasma atomic emission spectroscopy: 1.99 ± 0.08 ppm of boron (total) was detected at a conjugate quantity in the analyzed sample 0.036 µmol. It corresponds to 2.14 ± 0.09 of the HcyCo(B₉C₂H₁₁)₂ residues per albumin.

HSACy5HcyCo(B ₉ C ₂ H ₁₁ ) ₂ -MMAF and HSACy5HcyCo(B ₉ C ₂ H ₁₁ ) ₂ -MMAE. Purified HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ in PBS buffer (524 µL, 0.7 × 10^− 3 M, 0.37 µmol) was mixed with mc-vc-pub-MMAE or mc-vc-pub-MMAF dissolved in DMSO (52.4 µL and 2.8 µmol). The molar ratio peptide / HSA was 7.5, and a volume ratio DMSO / PBS in the reaction mixture was 0.1. The reaction was carried out for 18 h at 37°C. Purification of the final conjugates was performed out in the same way as for HSACy5HcyCo(B₉C₂H₁₁)₂. The yield of HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE ~ 86.77%. UV-vis (PBS buffer, pH 7.4): λ_max 278 nm (ε = (8.29 ± 0.1) × 10⁴), λ_max 646 nm (ε = (6.64 ± 0.1) × 10⁴). Mass spectrometry (MALDI-TOF) m/z: calculated for HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE 71026 Da. Mass spectrometry (MALDI-TOF) m/z: measured average MW for HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE is 70,615 Da corresponds to two residues of MMAE per one molecule of HSA (calculated MW for HcyCo(B₉C₂H₁₁)₂ 647 Da, calculated MW for mc-vc-pub-MMAE 1316 Da). The yield of HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF was ~ 84.8%. UV-vis (PBS buffer, pH 7.4): λ_max 278 nm (ε = (8.29 ± 0.1) × 104), λ_max 646 nm (ε = (6.64 ± 0.1) × 10⁴). Mass spectrometry (MALDI-TOF) m/z: calculated for HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ -MMAF 70951 Da. Mass spectrometry (MALDI-TOF) m/z: measured average MW for HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF is 70,643 Da corresponds to modification two residues of MMAF per one molecule of HSA (calculated MW for HcyCo(B₉C₂H₁₁)₂ 647 Da, calculated MW for mc-vc-pub-MMAF 1330 Da).

Cell viability assay (MTT test)

The effect of the modified protein samples on human glioma cell lines (U87 and T98G) was performed using the MTT assay [31]. The cells were grown to exponential growth phase further seeded in 96-well plates. Cell concentration was 2000 cells per well. Before treatment, the cells were incubated for 72 h. After that they were treated with medium containing albumin and its conjugates (HSA, HSACy5HcyCo(B₉C₂H₁₁)₂, HSACy5HcyCo(B₉C₂H₁₁)₂-MMAF, HSACy5HcyCo(B₉C₂H₁₁)₂-MMAE, HSA + mc-vc-pub-MMAF, HSA + mc-vc-pub-MMAE). Conjugate concentrations ranged from 0.02 to 30 µM, equivalent to the protein content. The treatment was performed at 37°C for 72 h. After that, MTT was added to a concentration of 0.5 mg/mL. After incubation at 37°C for 2 h, the medium was removed, and each well was added by 100 µL of isopropanol to dissolve the formazan crystals. The plate was analyzed using a Multiscan FC microplate reader (Thermo Fisher Scientific Corporation) with an absorbance peak at 570 nm. The absorption intensity at 620 nm was used as a baseline. Three independent tests for each protein sample were performed. Data are presented as means with standard deviations.

As a promising approach to improve the tumor selectivity of anticancer drugs, the prodrug is a bioreversible medication that is specifically converted to the active drug by chemical or enzymatic transformation in the tumor microenvironment, which can considerably reduce the chemotherapy-induced side effects [32, 33]. To harness the intrinsic transport properties of albumin yet improve the therapeutic index of current in situ albumin-binding prodrugs, authors [11] developed albumin-drug conjugates with a controlled loading that achieved better antitumor efficacy. Here, model drug monomethyl auristatin E (MMAE) was conjugated ex vivo to Cys34 of albumin via a cathepsin B-sensitive dipeptide linker to ensure that all drugs would be bound specifically to albumin. The utility of Cys34 in protein modification cannot be overstated. However, DTNB (5,5’-dithio-bis(2-nitrobenzoic acid)) titrations indicate the sulfhydryl titer for most commercial plasma HSA preparations is approximately 30–40% [34, 35]. In healthy subjects, Cys34 is mainly present in a reduced form (about 70%) (HSAred) while 25–30% is reversibly oxidized as a mixed disulfide, mainly with cysteine or in minor amounts with cysteinyl glycine, homocysteine and glutathione (HSAox) [35]. Very small amounts (3–4%) of irreversibly oxidized forms, e.g., sulfinate and sulfonate, are also found [33]. Pathologic conditions, like kidney or liver diseases, may increase the level of oxidized HSA to 70% [36, 37]. The heterogeneity of HSA is central to its physiological role and presents a complication for protein modification, but that is the biological reality. For the synthesis of albumin-drug conjugate with multiple payloads MMAE, a controlled reduction by TCEP was first used to expose more reactive thiols from disulfide bonds on albumin for conjugation [11]. However, partial reduction and subsequent addition of multiple drugs to albumin may affect the structure of albumin, which has been reflected in changes to the secondary structure of albumin-drug conjugate.

We previously reported using the reactivity of a thiolactone homocysteine (a cyclic thioester) as a latent thiol functionality in thiol-‘click’ chemistry for the synthesis of HSA-based theranostic agents [6, 7, 23, 24, 38]. The thiol was released by nucleophilic ring-opening (aminolysis) by amino groups on the HSA and subsequently reacted with a thiol ‘scavenger’ (a maleimide of the drug). Important aspect of our work is that by achieving an optimal drug-to-albumin ratio through site-specific conjugation, we minimize the change in structure to albumin, which is important for achieving antitumor efficacy [6, 7]. Similar to our work, other strategies on albumin-drug complexes have focused ex vivo covalent conjugation. For example, there was earlier literature that used the same MMAE payload and linker covalently conjugated to albumin [13, 14]. In this work, albumin was thiolated to allow for ~ 4 MMAE molecules per albumin and allow for conjugation for RGD peptide for cell targeting. However, this conjugate failed to retain the intrinsic properties of albumin due to its non-specific conjugation through lysine.

Here, we use a thiolactone derivative as a functional handle for site-specific coupling of a bis(dicarbollide) complex of cobalt (III) and auristatins to HSA. The construction of boron-albumin auristatin conjugates is illustrated in Scheme 2.

HSA was preliminarily modified with the Cy5 dye at the cysteine residue 34 according to the method [30] to obtain the HSA-Cy5 conjugate (Scheme 2, path a). The conjugation reaction of N-substituted boron-homocysteine thiolactone to HSA-Cy5 (Scheme 2, path b) was performed in PBS buffer (pH 7.4) at 37°C. Low-molecular-weight homocysteine derivatives were removed from the HSA conjugates by centrifugal filtration with Centricon concentrators having a molecular weight cut-off of 3,000 Da. The resulting conjugate HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ UV-Vis spectrum contains a band at 650 nm, which matches the presence of Cy5 dye in this structure (Fig. 1, panel A). The successful synthesis of HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ was confirmed by inductively coupled plasma atomic emission spectroscopy: 2.0 HcyCo(B₉C₂H₁₁)₂ residues per albumin on average.

Modification of HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ with maleimide auristatins (mc-vc-pab-MMAE and mc-vc-pab-MMAF) leads to a slight decrease in the mobility of the modified albumin conjugates in protein gel electrophoresis (Fig. 1, panel C), it can be explained by an increase in the mass of the conjugates (Fig. 1, panel B). The MALDI mass spectrometry data indicate mass increases of the HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ by 2633 and 2661 Da for HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE and HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF respectively (Fig. 1, panel B). This corresponds to the addition of 2 residues of each maleimide reagent per protein molecule.

In vitro cytotoxicity assay

MTT assays were utilized to evaluate the in vitro cellular proliferation inhibitions of HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE and HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF conjugates against human glioma cells. Glioma stem cells and other cells that exist in the glioma microenvironment play a crucial role in mediating glioma immune escape, tumor invasion, and recurrence [39]. The cysteine cathepsin family plays a prominent role in the immune escape of glioma [40–42]. A dipeptide (valine-citrulline) linker, cleavable by lysosomal proteases (e.g., cathepsin B), has been used us to link auristatins to boron-albumin. U87 and T98G cell lines were exposed to increasing albumin-based conjugates concentrations yielding dose-dependent proliferation inhibition after 72 hours of treatment (Fig. 2). The cytotoxicity of the HSA-Cy5-HcyCo(B₉C₂H₁₁)₂ conjugate, which was not modified with auristatin reagents, was insignificant in both cell lines. Auristatin-HSA conjugates showed improved cellular growth inhibition in cathepsin B overexpressed U87 and T98G cells compared to boron-containing albumin, indicating auristatins could be released and inhibit the proliferation of glioma cancer cells, which encourages us for further in vivo investigation.

Table 1

The half-maximal inhibitory concentration (IC₅₀) for HSA homocystamides and controls (mixtures HSA + MMAF, HSA + MMAE)
Cells	Sumple	IC₅₀	R
T98G	HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE	0.034	0.99
	HSA + MMAE	0.010	0.99
	HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF	0.147	0.99
	HSA + MMAF	0.044	0.98
U87	HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE	0.97	0.89
	HSA + MMAE	0.173	0.71
	HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF	1.16	0.96
	HSA + MMAF	1.02	0.80

Compared to the MMAF-albumin conjugate, the MMAE-albumin conjugate exhibited a 4–4.5-fold increase in potency when tested on T98G. Further, this conjugate was found to kill U87 cell type less effectively than T98G with IC₅₀ values of 0.97 µM (Table 1). Furthermore, taking into account the IC₅₀ values of free MMAE and free MMAF, we see that free MMAE is also more cytotoxic than the MMAF.

Monomethylauristatin F is an auristatin that possesses a negatively charged C-terminal phenylalanine residue that limits cell permeability, in contrast to monomethylauristatin E, which is uncharged and freely cell permeable [43]. Intracellular linker proteolysis of monomethylauristatin E conjugates may, therefore, expose surrounding normal tissues to free drug that may induce toxicity. The risk of toxicity will be reduced when MMAF-albumin conjugate is used. It is also plausible that the accumulation of albumin-drug conjugate within the cells will by far compensate for the differences in intrinsic activity, especially when prolonged uptake can be ensured, for instance, by ensuring that the receptor-mediated uptake is taking place efficiently. The delivery method of albumin to tumor tissues is passive because of the enhanced permeability and retention effect [44], but also active due to secreted protein acidic and rich in cysteine (SPARC) and gp60 receptors [45]. These receptors are known to be highly expressed in high-grade glioma cells, and treatment with albumin-containing compounds using SPARC, which is a target of active transport [46, 47]. Albumin can to target overexpressed gp-60 and SPARC receptors, allowing an enhanced drug uptake and bypassing drug efflux mechanisms. Moreover, it was found that increases in Caveolin-1 expression resulted in higher uptake of albumin [48]. Albumin enters through caveolae with the Fc-receptor, moves along actin, and reaches the early endosome, where some of them are sorted for lysosomal degradation, and others are directly transported outside the cells through exocytosis. The fact remains that as long as cancer cell biology is taken into account, albumin-binding proteins and caveolin-1–related roles seem to be tightly dependent on the cancer cell type. We believe that this may be responsible for the difference in IC₅₀ values for auristatin-HSA conjugates in various cancer cell types.

Albumin-driven delivery of therapeutics and imaging agents has become a popular technology, in parallel to antibody-driven targeting strategies. Recently, nano carrier-based boron delivery system, such as closo-dodecaborate-albumin conjugate, has been developed in order to achieve efficient BNCT. The conjugation of bimodal HSA with undecahydro-closo-dodecaborate little reduce human glioma cell line viability in the absence of irradiation but allowed for neutron capture and decreased tumor cell survival under epithermal neutron flux.

In this paper, we synthesized N-substituted boron-homocysteine thiolactone as a conjugation system for albumin functionalization by auristatins. The new N-acylated homocysteine thiolactone bearing a cobalt bis(dicarbollide) derivative was used to create the fluorophore-albumin based construct. Boron-homocysteine thiolactone was found to possess a high efficacy of conjugation to albumin. We report on the synthesis of a fluorophore-labeled boron-homocystamide conjugates of human serum albumin and their use in thiol-‘click’ chemistry to prepare a novel multifunctional constructs with the antitubulin agents MMAE or MMAF. We demonstrate that boron-equipped albumin conjugate with MMAE was more potent than MMAF conjugate, in the killing tumor cells.

The strategy of preparation of auristatin-modified boron-albumin conjugates proposed in this work could provide new ideas for the development of new generational albumin drug conjugates. Further studies are required to use them in a complete treatment of diseases.

Acknowledgements We thank the Joint Center for genomic, proteomic and metabolomics studies (ICBFM SB RAS) for obtaining mass-spectra.

Author contributions Study conception and design: V.N.S. and T.S.G.; syntheses: M.W. and I.A.M.;data collection: M.W., I.A.M., O.D.Z. and A.I.K.; analysis and interpretation of results: T.V.P and T.S.G.; draft manuscript preparation: T.V.P and T.S.G. All authors reviewed the results and approved the final version of the manuscript.

Funding This work was supported by the Russian state-funded project for ICBFM SB RAS (grant number 121031300042-1).

Data availability Original data is available from the authors upon request.

Ethics approval and consent to participate Not applicable.

Informed consent Not applicable.

Consent for publication Not applicable.

Research involving human participants or animals Not applicable.

Competing interests The authors declare no competing interests.

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Schemes 1-2 are available in the Supplementary Files section.

SupplWang2023InvestigationalNewDrugs.docx
Schemes.docx
Scheme 1. General synthetic route for the homocysteine thiolactone containing bis(dicarbollide) complex of cobalt (III). Reagents and conditions: (a) — 1) 5% alcohol solution sodium hydroxide, boiling, 12 h, 2) 1 M HCl, 3)H₂O, Me₃NHCl; (b) —40% aqueous sodium hydroxide; (c) — 1) CoSO₄ × 7 H₂O (1.2 excess), 30 min, 2) water solution of CsCl; (d) — BF₃ × Et₂O (8.3 excess) in dioxane, boiling, 5 h; (e) — 3 × 10^‑4 M K₂CO₃ in acetone, methyl ether of p-hydroxybenzoic acid (2.9 excess), 60 °C, 1 h; (f) — 1 M KOH, 1 day; (g) — pentafluorophenol (1.08 excess), DCC (1.04 excess) in ethyl acetate, 4 h at room temperature; (h) — DL-HTL × HCl (1.1 excess), DIPEA (1.46 excess) in DMF, 60 °C, 4 h. Scheme 2. The constructing pathway of the new conjugates for BNCT: HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAF and HSA-Cy5-HcyCo(B₉C₂H₁₁)₂-MMAE.

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Development of theranostics albumin auristatin conjugates for combining chemotherapy with boron neutron capture therapy

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Abstract

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Introduction

Materials and Methods

Chemicals, reagents, and facilities

Synthesis of the homocysteine thiolactone containing bis(dicarbollide) complex of cobalt (III)

Synthesis and characterization of multifunctional human serum albumin-therapeutic conjugates

Cell viability assay (MTT test)

Results and discussion

In vitro cytotoxicity assay

Conclusions

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References

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Supplementary Files

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